Substituted N-(Tetrazol-5-yl)- and N-(Triazol-5-yl)arylcarboxamide Compounds and Their Use as Herbicides

ABSTRACT

The present invention relates to a triazole compound of formula I, an N-oxide or an agriculturally suitable salt thereof, wherein the variables are defined as in the specification. The invention further refers to a composition comprising such compound and to the use thereof for controlling unwanted vegetation.

The present invention relates to substituted N-(tetrazol-5-yl)- andN-(triazol-5-yl)arylcarboxamide compounds and the N-oxides and saltsthereof and to compositions comprising the same. The invention alsorelates to the use of the N-(tetrazol-5-yl)- andN-(triazol-5-yl)arylcarboxamide compounds or of the compositionscomprising such compounds for controlling unwanted vegetation.Furthermore, the invention relates to methods of applying suchcompounds.

For the purposes of controlling unwanted vegetation, especially incrops, there is an ongoing need for new herbicides which have highactivities and selectivities together with a substantial lack oftoxicity for humans and animals.

WO 2011/035874 describes N-(1,2,5-oxadiazol-3-yl)benzamides carrying 3substituents in the 2-, 3- and 4-positions of the phenyl ring and theiruse as herbicides.WO 2012/028579 describes N-(tetrazol-4-yl)- andN-(triazol-3-yl)arylcarboxylic acid amides carrying 3 substituents inthe 2-, 3- and 4-positions of the aryl ring and their use as herbicides.

The compounds of the prior art often suffer form insufficient herbicidalactivity in particular at low application rates and/or unsatisfactoryselectivity resulting in a low compatibility with crop plants.

Accordingly, it is an object of the present invention to provide furtherN-(tetrazol-5-yl)- and N-(triazol-5-yl)arylcarboxamide compounds havinga strong herbicidal activity, in particular even at low applicationrates, a sufficiently low toxicity for humans and animals and/or a highcompatibility with crop plants. The N-(tetrazol-5-yl)- andN-(triazol-5-yl)arylcarboxamide compounds should also show a broadactivity spectrum against a large number of different unwanted plants.These and further objectives are achieved by the compounds of formula Idefined below and their N-oxides and also their agriculturally suitablesalts.

It has been found that the above objectives can be achieved bysubstituted N-(tetrazol-5-yl)- and N-(triazol-5-yl)arylcarboxamidecompounds of the general formula I, as defined below, including theirN-oxides and their salts, in particular their agriculturally suitablesalts. Therefore, in a first aspect the present invention relates tocompounds of formula I,

an N-oxide or an agriculturally suitable salt thereof,

wherein

R¹ is selected from the group consisting of halogen, C₁-C₈-alkyl,C₁-C₈-haloalkyl, nitro, C₁-C₄-alkoxy-C₁-C₄-alkyl, cyano-Z¹,C₂-C₈-alkenyl, C₂-C₈-alkynyl, C₃-C₁₀-cycloalkyl-Z¹, C₂-C₈-haloalkenyl,C₃-C₈-haloalkynyl, C₁-C₈-alkoxy, C₁-C₄-alkoxy-C₁-C₄-alkoxy-Z¹,C₁-C₄-alkylthio-C₁-C₄-alkyl, C₁-C₄-alkylthio-C₁-C₄-alkylthio-Z¹,C₂-C₆-alkenyloxy, C₂-C₆-alkynyloxy, C₁-C₆-haloalkoxy,C₁-C₄-haloalkoxy-C₁-C₄-alkyl, C₁-C₄-haloalkoxy-C₁-C₄-alkoxy-Z¹,R^(1b)—S(O)_(k)—Z¹, phe-noxy-Z¹ and heterocyclyloxy-Z¹, whereheterocyclyloxy is an oxygen bound 5- or 6-membered monocyclic or 8-, 9-or 10-membered bicyclic saturated, partially unsaturated or aromaticheterocycle, which contains 1, 2, 3 or 4 heteroatoms as ring members,which are selected from the group consisting of O, N and S, where thecyclic groups in phenoxy and heterocyclyloxy are unsubstituted orsubstituted by 1, 2, 3 or 4 groups R¹¹, which are identical ordifferent;

X is N or CR²;

R² is selected from the group consisting of hydrogen, halogen,hydroxy-Z², nitro, C₁-C₄-nitroalkyl, cyano, C₁-C₄-cyanoalkyl,C₁-C₆-alkyl, C₂-C₈-alkenyl, C₂-C₈-alkynyl, C₃-C₁₀-cycloalkyl-Z²,C₃-C₁₀-cycloalkoxy-Z², where the C₃-C₁₀-cycloalkyl groups in the twoaforementioned radicals are unsubstituted or partially or completelyhalogenated, C₁-C₈-haloalkyl, C₂-C₈-haloalkenyl, C₃-C₈-haloalkynyl,C₁-C₈-alkoxy-Z², C₁-C₈-haloalkoxy-Z², C₃-C₁₀-cycloalkyl-C₁-C₂-alkoxy,C₁-C₄-alkoxy-C₁-C₄-alkoxy-Z², C₁-C₄-alkylthio-C₁-C₄-alkylthio-Z²,C₂-C₈-alkenyloxy-Z², C₂-C₈-alkynyloxy-Z², C₂-C₈-haloalkenyloxy-Z²,C₃-C₈-haloalkynyloxy-Z², C₁-C₄-haloalkoxy-C₁-C₄-alkoxy-Z²,(tri-C₁-C₄-alkyl)silyl-Z², R^(2b)—S(O)_(k)—Z², R^(2c)—C(═O)—Z²,R^(2d)O—C(═O)—Z², R^(2d)O—N═CH—Z², R^(2d)O—N═CC₁-C₄-alkyl-Z²,R^(2d)O—N═CC₁-C₄-haloalkyl-Z², R^(2c)R^(2d)C═N—O—C₁-C₄-alkyl,R^(2e)R^(2f)N—C(═O)—Z², R^(2g)R^(2h)N—Z², phenyl-Z^(2a),heterocyclyl-Z^(2a), where heterocyclyl is a 3-, 4-, 5- or 6-memberedmonocyclic or 8-, 9- or 10-membered bicyclic saturated, partiallyunsaturated or aromatic heterocycle, which contains 1, 2, 3 or 4heteroatoms as ring members, which are selected from the groupconsisting of O, N and S, where the cyclic groups in phenyl-Z^(2a) andheterocyclyl-Z^(2a) are unsubstituted or substituted by 1, 2, 3 or 4groups R²¹, which are identical or different, rhodano,C₃-C₆-cycloalkenyl, OC(O)OR²², OC(O)N(R²²)₂, ONC(R²³)₂, OSO₂R²⁵,SO₂OR²², SO₂N(R²²)₂, N(R²²)C(O)OR²², N(R²²)C(O)N(R²²)₂, C(O)N(R²²)OR²²,P(O)(O—C₁-C₄-alkyl)₂, C₁-C₆-alkyl-OC(O)R²², C₁-C₆-alkyl-OSO₂R²⁵,C₁-C₆-alkyl-SO₂OR²², C₁-C₆-alkyl-SO₂N(R²²)₂,C₁-C₆-alkyl-P(O)(O—C₁-C₄-alkyl)₂,

R³ is selected from the group consisting of hydrogen, halogen,hydroxy-Z², nitro, C₁-C₄-nitroalkyl, cyano, C₁-C₄-cyanoalkyl,C₁-C₆-alkyl, C₂-C₈-alkenyl, C₂-C₈-alkynyl, C₃-C₁₀-cycloalkyl-Z²,C₃-C₁₀-cycloalkoxy-Z², where the C₃-C₁₀-cycloalkyl groups in the twoaforementioned radicals are unsubstituted or partially or completelyhalogenated, C₁-C₈-haloalkyl, C₂-C₈-haloalkenyl, C₃-C₈-haloalkynyl,C₁-C₈-alkoxy-Z², C₁-C₈-haloalkoxy-Z², C₃-C₁₀-cycloalkyl-C₁-C₂-alkoxy,C₁-C₄-alkoxy-C₁-C₄-alkoxy-Z², C₁-C₄-alkylthio-C₁-C₄-alkylthio-Z²,C₂-C₈-alkenyloxy-Z², C₂-C₈-alkynyloxy-Z², C₂-C₈-haloalkenyloxy-Z²,C₃-C₈-haloalkynyloxy-Z², C₁-C₄-haloalkoxy-C₁-C₄-alkoxy-Z²,(tri-C₁-C₄-alkyl)silyl-Z², R^(2b)—S(O)_(k)—Z², R^(2c)—C(═O)—Z²,R^(2d)O—C(═O)—Z², R^(2d)O—N═CH—Z², R^(2c)R^(2d)C═N—O—C₁-C₄-alkyl,R^(2e)R^(2f)N—C(═O)—Z², R^(2g)R^(2h)N—Z², phenyl-Z^(2a),heterocyclyl-Z^(2a), where heterocyclyl is a 3-, 4-, 5- or 6-memberedmonocyclic or 8-, 9- or 10-membered bicyclic saturated, partiallyunsaturated or aromatic heterocycle, which contains 1, 2, 3 or 4heteroatoms as ring members, which are selected from the groupconsisting of O, N and S, where the cyclic groups in phenyl-Z^(2a) andheterocyclyl-Z^(2a) are unsubstituted or substituted by 1, 2, 3 or 4groups R²¹, which are identical or different, rhodano,C₃-C₆-cycloalkenyl, C₃-C₆-halocycloalkenyl,C₃-C₆-cycloalkenyl-C₁-C₆-alkyl, C₃-C₆-halocycloalkenyl-C₁-C₆-alkyl,OC(O)R²², OC(O)OR²⁵, OC(O)N(R²²)₂, OSO₂R²⁵, SO₂OR²², SO₂N(R²²)₂,SO₂N(R²²)C(O)R²², SO₂N(R²²)C(O)OR²⁵, SO₂N(R²²)C(O)N(R²²)₂,N(R²²)C(O)OR²⁵, N(R²²)C(O)N(R²²)₂, N(R²²)S(O)₂OR²², N(R²²)S(O)₂N(R²²)₂,C(O)N(R²²)OR²², C(O)N(R²²)N(R²²)₂, C(O)N(R²²)C(O)R²²,C(O)N(R²²)C(O)OR²⁵, C(O)N(R²²)C(O)N(R²²)₂, C(O)N(R²²)SO₂R²⁵,C(O)N(R²²)SO₂OR²², C(O)N(R²²)SO₂N(R²²)₂, P(O)(OH)₂,P(O)(O—C₁-C₄-alkyl)₂, C₁-C₆-alkyl-OC(O)R²², C₁-C₆-alkyl-OC(O)OR²⁵,C₁-C₆-alkyl-OC(O)N(R²²)₂, C₁-C₆-alkyl-OSO₂R²⁵, C₁-C₆-alkyl-SO₂OR²²,C₁-C₆-alkyl-SO₂N(R²²)₂, C₁-C₆-alkyl-SO₂N(R²²)C(O)R²²,C₁-C₆-alkyl-SO₂N(R²²)C(O)OR²⁵, C₁-C₆-alkyl-SO₂N(R²²)C(O)N(R²²)₂,C₁-C₆-alkyl-N(R²²)C(O)OR²⁵, C₁-C₆-alkyl-N(R²²)C(O)N(R²²)₂,C₁-C₆-alkyl-N(R²²)S(O)₂OR²², C₁-C₆-alkyl-N(R²²)S(O)₂N(R²²)₂,C₁-C₆-alkyl-C(O)N(R²²)OR²², C₁-C₆-alkyl-C(O)N(R²²)N(R²²)₂,C₁-C₆-alkyl-C(O)N(R²²)C(O)R²², C₁-C₆-alkyl-C(O)N(R²²)C(O)OR²⁵,C₁-C₆-alkyl-C(O)N(R²²)C(O)N(R²²)₂, C₁-C₆-alkyl-C(O)N(R²²)SO₂R²⁵,C₁-C₆-alkyl-C(O)N(R²²)SO₂OR²², C₁-C₆-alkyl-C(O)N(R²²)SO₂N(R²²)₂,C₁-C₆-alkyl-P(O)(OH)₂ and C₁-C₆-alkyl-P(O)(O—C₁-C₄-alkyl)₂;

R⁴ is selected from the group consisting of hydrogen, halogen,C₁-C₈-alkyl, cyano-Z¹, nitro, C₃-C₇-cycloalkyl,C₃-C₇-cycloalkyl-C₁-C₄-alkyl, where the C₃-C₇-cycloalkyl groups in thetwo aforementioned radicals are unsubstituted or partially or completelyhalogenated, C₂-C₈-alkenyl, C₂-C₈-alkynyl, C₁-C₈-haloalkyl,C₁-C₃-alkylamino, C₁-C₃-dialkylamino, C₁-C₃-alkylamino-S(O)_(k),C₁-C₃-alkylcarbonyl, C₁-C₈-alkoxy, C₁-C₄-alkoxy-C₁-C₄-alkyl,C₁-C₄-alkoxy-C₁-C₄-alkoxy-Z¹, C₁-C₄-alkylthio-C₁-C₄-alkyl,C₁-C₄-alkylthio-C₁-C₄-alkylthio-Z¹, C₂-C₆-alkenyloxy, C₂-C₆-alkynyloxy,C₁-C₆-haloalkoxy, C₁-C₄-haloalkoxy-C₁-C₄-alkyl,C₁-C₄-haloalkoxy-C₁-C₄-alkoxy-Z¹, R^(1b)—S(O)_(k)—Z¹, phenoxy-Z¹ andheterocyclyloxy-Z¹, where heterocyclyloxy is an oxygen bound 5- or6-membered monocyclic or 8-, 9- or 10-membered bicyclic saturated,partially unsaturated or aromatic heterocycle, which contains 1, 2, 3 or4 heteroatoms as ring members, which are selected from the groupconsisting of O, N and S, where the cyclic groups in phenoxy andheterocyclyloxy are unsubstituted or substituted by 1, 2, 3 or 4 groupsR¹¹, which are identical or different; R⁵ is selected from the groupconsisting of halogen, cyano-Z¹, nitro, C₁-C₈-alkyl, C₃-C₇-cycloalkyl,C₃-C₇-cycloalkyl-C₁-C₄-alkyl, where the C₃-C₇-cycloalkyl groups in thetwo aforementioned radicals are unsubstituted or partially or completelyhalogenated, C₂-C₈-alkenyl, C₂-C₈-alkynyl, C₁-C₈-haloalkyl,C₁-C₃-alkylamino, C₁-C₃-dialkylamino, C₁-C₃-alkylamino-S(O)_(k),C₁-C₃-alkylcarbonyl, C₁-C₈-alkoxy, C₁-C₄-alkoxy-C₁-C₄-alkyl,C₁-C₄-alkoxy-C₁-C₄-alkoxy-Z¹, C₁-C₄-alkylthio-C₁-C₄-alkyl,C₁-C₄-alkylthio-C₁-C₄-alkylthio-Z¹, C₂-C₆-alkenyloxy, C₂-C₆-alkynyloxy,C₁-C₆-haloalkoxy, C₁-C₄-haloalkoxy-C₁-C₄-alkyl,C₁-C₄-haloalkoxy-C₁-C₄-alkoxy-Z¹, R^(1b)—S(O)_(k)—Z¹, phenoxy-Z¹ andheterocyclyloxy-Z¹, where heterocyclyloxy is an oxygen bound 5- or6-membered monocyclic or 8-, 9- or 10-membered bicyclic saturated,partially unsaturated or aromatic heterocycle, which contains 1, 2, 3 or4 heteroatoms as ring members, which are selected from the groupconsisting of O, N and S, where the cyclic groups in phenoxy andheterocyclyloxy are unsubstituted or substituted by 1, 2, 3 or 4 groupsR¹¹, which are identical or different;

R⁶ is selected from the group consisting of cyano, nitro, hydroxy,amino, C₁-C₆-alkyl, C₁-C₆-cyano-alkyl, C₃-C₇-cycloalkyl,C₃-C₇-cycloalkyl-C₁-C₄-alkyl, where the C₃-C₇-cycloalkyl groups in thetwo aforementioned radicals are unsubstituted or partially or completelyhalogenated, C₁-C₆-haloalkyl, C₁-C₆-alkoxy, C₁-C₆-alkylcarbonyl,C₁-C₆-alkyaminocarbonyl, C₁-C₆-dialkyl-aminocarbonyl, C₁-C₆-alkyamino,C₁-C₆-dialkyl-amino, C₂-C₆-alkenyl, C₂-C₆-haloalkenyl, C₂-C₆-alkynyl,C₂-C₆-haloalkynyl, C₁-C₄-alkoxy-C₁-C₄-alkyl,C₁-C₄-haloalkoxy-C₁-C₄-alkyl, R^(b)R^(b)N—S(O)_(n)—Z, R^(b)O—S(O)_(n)—Z,R^(b)—S(O)_(n)—Z, R^(c)R^(c)N—C₁-C₃-alkyl-S(O)_(n)—C₁-C₃-alkyl,R^(c)—C(═O)—C₁-C₃-alkyl, R^(d)—C(═O)O—C₁-C₃-alkyl,R^(d)—O—C(═O)O—C₁-C₃-alkyl, R^(d)O—C(═O)—C₁-C₃-alkyl,R^(e)R^(f)N—C(═O)—C₁-C₃-alkyl, R^(c)—C(═O)R^(e)N—C₁-C₃-alkyl,R^(b)—S(O)_(n)—R^(e)N—C₁-C₃-alkyl, R^(c)R^(c)N—C₁-C₃-alkyl, phenyl-Z andheterocyclyl-Z, where heterocyclyl is a 5- or 6-membered monocyclic or8-, 9- or 10-membered bicyclic saturated, partially unsaturated oraromatic heterocycle, which contains 1, 2, 3 or 4 heteroatoms as ringmembers, which are selected from the group consisting of O, N and S,where phenyl and heterocyclyl are unsubstituted or substituted by 1, 2,3 or 4 groups R′, which are identical or different;

R⁷ is selected from the group consisting of hydrogen, C₁-C₆-alkyl,C₃-C₇-cycloalkyl, C₃-C₇-cycloalkyl-C₁-C₄-alkyl, where theC₃-C₇-cycloalkyl groups in the two aforementioned radicals areunsubstituted or partially or completely halogenated, C₁-C₆-haloalkyl,C₂-C₆-alkenyl, C₂-C₆-haloalkenyl, C₂-C₆-alkynyl, C₂-C₆-haloalkynyl,C₁-C₄-alkoxy-C₁-C₄-alkyl, C₁-C₄-haloalkoxy-C₁-C₄-alkyl,R^(b)—S(O)_(n)—C₁-C₃-alkyl, R^(c)—C(═O)—C₁-C₃-alkyl,R^(d)O—C(═O)—C₁-C₃-alkyl, R^(e)R^(f)N—C(═O)—C₁-C₃-alkyl,R^(g)R^(h)N—C₁-C₃-alkyl, phenyl-Z and heterocyclyl-Z, where heterocyclylis a 5- or 6-membered monocyclic or 8-, 9- or 10-membered bicyclicsaturated, partially unsaturated or aromatic heterocycle, which contains1, 2, 3 or 4 heteroatoms as ring members, which are selected from thegroup consisting of O, N and S, where phenyl and heterocyclyl areunsubstituted or substituted by 1, 2, 3 or 4 groups R′, which areidentical or different;

B is N or CH;

R′, R¹¹, R²¹ independently of each other are selected from the groupconsisting of halogen, NO₂, ON, C₁-C₆-alkyl, C₃-C₇-cycloalkyl,C₃-C₇-halocycloalkyl, C₁-C₆-haloalkyl, C₂-C₆-alkenyl, C₂-C₆-haloalkenyl,C₂-C₆-alkynyl, C₂-C₆-haloalkynyl, C₁-C₆-alkoxy,C₁-C₄-alkoxy-C₁-C₄-alkyl, C₁-C₄-alkylthio-C₁-C₄-alkyl,C₁-C₄-haloalkoxy-C₁-C₄-alkyl, C₁-C₄-alkoxy-C₁-C₄-alkoxy,C₃-C₇-cycloalkoxy and C₁-C₆-haloalkyloxy, or two vicinal radicals R′,R¹¹ or R²¹ together may form a group ═O;

Z, Z¹, Z² independently of each other are selected from the groupconsisting of a covalent bond and C₁-C₄-alkanediyl;

Z^(2a) is s Z^(2a) elected from the group consisting of a covalent bond,C₁-C₄-alkanediyl, O—C₁-C₄-alkanediyl, C₁-C₄-alkanediyl-O andC₁-C₄-alkanediyl-O—C₁-C₄-alkanediyl;

R^(b), R^(1b), R^(2b) independently of each other are selected from thegroup consisting of C₁-C₆-alkyl, C₃-C₇-cycloalkyl, C₁-C₆-haloalkyl,C₂-C₆-alkenyl, C₂-C₆-haloalkenyl, C₂-C₆-alkynyl, C₂-C₆-haloalkynyl,phenyl and heterocyclyl, where heterocyclyl is a 5- or 6-memberedmonocyclic saturated, partially unsaturated or aromatic heterocycle,which contains 1, 2, 3 or 4 heteroatoms as ring members, which areselected from the group consisting of O, N and S, where phenyl andheterocyclyl are unsubstituted or substituted by 1, 2, 3 or 4 groups,which are identical or different and selected from the group consistingof halogen, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy andC₁-C₄-haloalkoxy;

R^(c), R^(2c) independently of each other are selected from the groupconsisting of hydrogen, C₁-C₆-alkyl, C₃-C₇-cycloalkyl,C₃-C₇-cycloalkyl-C₁-C₄-alkyl, where the C₃-C₇-cycloalkyl groups in thetwo aforementioned radicals are unsubstituted or partially or completelyhalogenated, C₁-C₆-haloalkyl, C₂-C₆-alkenyl, C₂-C₆-haloalkenyl,C₂-C₆-alkynyl, C₂-C₆-haloalkynyl, C₁-C₄-alkoxy-C₁-C₄-alkyl, phenyl,benzyl and heterocyclyl, where heterocyclyl is a 5- or 6-memberedmonocyclic saturated, partially unsaturated or aromatic heterocycle,which contains 1, 2, 3 or 4 heteroatoms as ring members, which areselected from the group consisting of O, N and S, where phenyl, benzyland heterocyclyl are unsubstituted or substituted by 1, 2, 3 or 4groups, which are identical or different and selected from the groupconsisting of halogen, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy andC₁-C₄-haloalkoxy;

R^(d), R^(2d) independently of each other are selected from the groupconsisting of C₁-C₆-alkyl, C₃-C₇-cycloalkyl,C₃-C₇-cycloalkyl-C₁-C₄-alkyl, where the C₃-C₇-cycloalkyl groups in thetwo aforementioned radicals are unsubstituted or partially or completelyhalogenated, C₁-C₆-haloalkyl, C₂-C₆-alkenyl, C₂-C₆-haloalkenyl,C₂-C₆-alkynyl, C₂-C₆-haloalkynyl, C₁-C₄-alkoxy-C₁-C₄-alkyl, phenyl andbenzyl, where phenyl and benzyl are unsubstituted or substituted by 1,2, 3 or 4 groups, which are identical or different and selected from thegroup consisting of halogen, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxyand C₁-C₄-haloalkoxy;

R^(e), R^(f) independently of each other are selected from the groupconsisting of hydrogen, C₁-C₆-alkyl, C₃-C₇-cycloalkyl,C₃-C₇-cycloalkyl-C₁-C₄-alkyl, where the C₃-C₇-cycloalkyl groups in thetwo aforementioned radicals are unsubstituted or partially or completelyhalogenated, C₁-C₆-haloalkyl, C₂-C₆-alkenyl, C₂-C₆-haloalkenyl,C₂-C₆-alkynyl, C₂-C₆-haloalkynyl, C₁-C₄-alkoxy-C₁-C₄-alkyl, phenyl andbenzyl, where phenyl and benzyl are unsubstituted or substituted by 1,2, 3 or 4 groups, which are identical or different and selected from thegroup consisting of halogen, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxyand C₁-C₄-haloalkoxy, or

R^(e), R^(f) together with the nitrogen atom, to which they are boundmay form a 5-, 6 or 7-membered, saturated or unsaturated N-boundheterocyclic radical, which may carry as a ring member a furtherheteroatom selected from O, S and N and which is unsubstituted or maycarry 1, 2, 3 or 4 groups, which are identical or different and selectedfrom the group consisting of halogen, C₁-C₄-alkyl, C₁-C₄-haloalkyl,C₁-C₄-alkoxy and C₁-C₄-haloalkoxy;

R^(2e), R^(2f) independently of each other have the meanings given forR^(e), R^(f);

R^(g) is selected from the group consisting of hydrogen, C₁-C₆-alkyl,C₃-C₇-cycloalkyl, C₃-C₇-cycloalkyl-C₁-C₄-alkyl, where theC₃-C₇-cycloalkyl groups in the two aforementioned radicals areunsubstituted or partially or completely halogenated, C₁-C₆-haloalkyl,C₂-C₆-alkenyl, C₂-C₆-haloalkenyl, C₂-C₆-alkynyl, C₂-C₆-haloalkynyl,C₁-C₄-alkoxy-C₁-C₄-alkyl, C₁-C₄-alkylsulfonyl, C₁-C₄-alkylcarbonyl,phenyl and benzyl, where phenyl and benzyl are unsubstituted orsubstituted by 1, 2, 3 or 4 groups, which are identical or different andselected from the group consisting of halogen, C₁-C₄-alkyl,C₁-C₄-haloalkyl, C₁-C₄-alkoxy and C₁-C₄-haloalkoxy;

R^(h) is selected from the group consisting of hydrogen, C₁-C₆-alkyl,C₃-C₇-cycloalkyl, C₃-C₇-cycloalkyl-C₁-C₄-alkyl, where theC₃-C₇-cycloalkyl groups in the two aforementioned radicals areunsubstituted or partially or completely halogenated, C₁-C₆-haloalkyl,C₂-C₆-alkenyl, C₂-C₆-haloalkenyl, C₂-C₆-alkynyl, C₂-C₆-haloalkynyl,C₁-C₄-alkoxy-C₁-C₄-alkyl, C₁-C₄-alkylsulfonyl, C₁-C₄-alkylcarbonyl, aradical C(═O)—R^(k), phenyl and benzyl, where phenyl and benzyl areunsubstituted or substituted by 1, 2, 3 or 4 groups, which are identicalor different and selected from the group consisting of halogen,C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy and C₁-C₄-haloalkoxy, or

R^(g), R^(h) together with the nitrogen atom, to which they are boundmay form a 5-, 6 or 7-membered, saturated or unsaturated N-boundheterocyclic radical, which may carry as a ring member a furtherheteroatom selected from O, S and N and which is unsubstituted or maycarry 1, 2, 3 or 4 groups, which are identical or different and selectedfrom the group consisting of ═O, halogen, C₁-C₄-alkyl, C₁-C₄-haloalkyl,C₁-C₄-alkoxy and C₁-C₄-haloalkoxy;

R^(2g), R^(2h) independently of each other have the meanings given forR^(g), R^(h);

R^(k) has the meanings given for R^(c);

R²² is selected from the group consisting of hydrogen, C₁-C₆-alkyl,C₁-C₆-haloalkyl, C₂-C₆-alkenyl, C₂-C₆-haloalkenyl, C₂-C₆-alkynyl,C₃-C₆-haloalkynyl, C₃-C₆-cycloalkyl, C₃-C₆-cycloalkenyl,C₃-C₆-halocycloalkyl, C₃-C₆-cycloalkyl-C₁-C₆-alkyl,C₁-C₆-alkoxy-C₁-C₆-alkyl, C₃-C₆-cycloalkyl-C₁-C₆-alkoxy-C₁-C₆-alkyl,phenyl, phenyl-C₁-C₆-alkyl, heteroaryl, heteroaryl-C₁-C₆-alkyl,heterocyclyl, heterocyclyl-C₁-C₆-alkyl, phenyl-O—C₁-C₆-alkyl,heteroaryl-O—C₁-C₆-alkyl, heterocyclyl-O—C₁-C₆-alkyl,phenyl-N(R²³)—C₁-C₆-alkyl, heteroaryl-N(R²³)—C₁-C₆-alkyl,heterocyclyl-N(R²³)—C₁-C₆-alkyl, phenyl-S(O)_(n)—C₁-C₆-alkyl,heteroaryl-S(O)_(n)—C₁-C₆-alkyl, heterocyclyl-S(O)_(n)—C₁-C₆-alkyl,where the 15 aforementioned radicals are substituted by s residuesselected from the group consisting of nitro, halogen, cyano, rhodano,C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₃-C₆-cycloalkyl, C(O)OR²³, C(O)N(R²³)₂,OR²³, N(R²³)₂, S(O)_(n)R²⁴, S(O)₂OR²³, S(O)₂N(R²³)₂ andR²³O—C₁-C₆-alkyl, and where heterocyclyl bears 0, 1 or 2 oxo groups;

R²³ is selected from the group consisting of hydrogen, C₁-C₆-alkyl,C₁-C₆-haloalkyl, C₂-C₆-alkenyl, C₂-C₆-alkynyl, C₃-C₆-cycloalkyl,C₃-C₆-cycloalkyl-C₁-C₆-alkyl and phenyl;

R²⁴ is selected from the group consisting of C₁-C₆-alkyl,C₁-C₆-haloalkyl, C₂-C₆-alkenyl, C₂-C₆-alkynyl, C₃-C₆-cycloalkyl,C₃-C₆-cycloalkyl-C₁-C₆-alkyl and phenyl;

R²⁵ is selected from the group consisting of C₁-C₆-alkyl,C₁-C₆-haloalkyl, C₂-C₆-alkenyl, C₂-C₆-haloalkenyl, C₂-C₆-alkynyl,C₃-C₆-haloalkynyl, C₃-C₆-cycloalkyl, C₃-C₆-cycloalkenyl,C₃-C₆-halocycloalkyl, C₃-C₆-cycloalkyl-C₁-C₆-alkyl,C₁-C₆-alkoxy-C₁-C₆-alkyl, C₃-C₆-cycloalkyl-C₁-C₆-alkoxy-C₁-C₆-alkyl,phenyl, phenyl-C₁-C₆-alkyl, heteroaryl, heteroaryl-C₁-C₆-alkyl,heterocyclyl, heterocyclyl-C₁-C₆-alkyl, phenyl-O—C₁-C₆-alkyl,heteroaryl-O—C₁-C₆-alkyl, heterocyclyl-O—C₁-C₆-alkyl,phenyl-N(R²³)—C₁-C₆-alkyl, heteroaryl-N(R²³)—C₁-C₆-alkyl,heterocyclyl-N(R²³)—C₁-C₆-alkyl, phenyl-S(O)_(n)—C₁-C₆-alkyl,heteroaryl-S(O)_(n)—C₁-C₆-alkyl, heterocyclyl-S(O)_(n)—C₁-C₆-alkyl,where the 15 aforementioned radicals are substituted by s residuesselected from the group consisting of nitro, halogen, cyano, rhodano,C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₃-C₆-cycloalkyl, C(O)OR²³, C(O)N(R²³)₂,OR²³, N(R²³)₂, S(O)_(n)R²⁴, S(O)₂OR²³, S(O)₂N(R²³)₂ andR²³O—C₁-C₆-alkyl, and where heterocyclyl bears 0, 1 or 2 oxo groups;

R²⁶ is C₁-C₆-alkyl or C₁-C₄-alkoxy-C₁-C₄-alkyl;

R²⁷ is selected from the group consisting of hydrogen, cyano andC₁-C₄-haloalkylcarbonyl;

R²⁸, R²⁹ independently of each other are C₁-C₆-alkyl, or

R²⁸, R²⁹ together with the sulfur atom, to which they are bound may forma 5- or 6-membered saturated ring, which may carry as a ring member 1oxygen atom;

k is 0, 1 or 2;

n is 0, 1 or 2;

s is 0, 1, 2 or 3;

t is 0 or 1.

The compounds of the present invention, i.e. the compounds of formula I,their N-oxides, or their salts are particularly useful for controllingunwanted vegetation. Therefore, the invention also relates to the use ofa compound of the present invention, an N-oxide or a salt thereof or ofa composition comprising at least one compound of the invention, anN-oxide or an agriculturally suitable salt thereof for combating orcontrolling unwanted vegetation.

The invention also relates to a composition comprising at least onecompound according to the invention, including an N-oxide or a saltthereof, and at least one auxiliary. In particular, the inventionrelates to an agricultural composition comprising at least one compoundaccording to the invention including an N-oxide or an agriculturallysuitable salt thereof, and at least one auxiliary customary for cropprotection formulations.

The present invention also relates to a method for combating orcontrolling unwanted vegetation, which method comprises allowing aherbicidally effective amount of at least one compound according to theinvention, including an N-oxide or a salt thereof, to act on unwantedplants, their seed and/or their habitat.

Depending on the substitution pattern, the compounds of formula I mayhave one or more centers of chirality, in which case they are present asmixtures of enantiomers or diastereomers. The invention provides boththe pure enantiomers or pure diastereomers of the compounds of formulaI, and their mixtures and the use according to the invention of the pureenantiomers or pure diastereomers of the compound of formula I or itsmixtures. Suitable compounds of formula I also include all possiblegeometrical stereoisomers (cis/trans isomers) and mixtures thereof.

Cis/trans isomers may be present with respect to an alkene,carbon-nitrogen double-bond, nitrogen-sulfur double bond or amide group.The term “stereoisomer(s)” encompasses both optical isomers, such asenantiomers or diastereomers, the latter existing due to more than onecenter of chirality in the molecule, as well as geometrical isomers(cis/trans isomers).

Depending on the substitution pattern, the compounds of formula I may bepresent in the form of their tautomers. Hence the invention also relatesto the tautomers of the formula I and the stereoisomers, salts andN-oxides of said tautomers.

The term “N-oxide” includes any compound of the present invention whichhas at least one tertiary nitrogen atom that is oxidized to an N-oxidemoiety. N-oxides in compounds of formula I can in particular be preparedby oxidizing the ring nitrogen atom(s) of theN-(1,2,4-triazol-3-yl)arylcarboxamide ring with a suitable oxidizingagent, such as peroxo carboxylic acids or other peroxides, or the ringnitrogen atom(s) of a heterocyclic substituent R, R¹, R² or R³.

The present invention moreover relates to compounds as defined herein,wherein one or more of the atoms depicted in formula I have beenreplaced by its stable, preferably non-radioactive isotope (e.g.,hydrogen by deuterium, ¹²C by ¹³C, ¹⁴N by ¹⁵N, ¹⁶O by ¹⁸O) and inparticular wherein at least one hydrogen atom has been replaced by adeuterium atom. Of course, the compounds according to the inventioncontain more of the respective isotope than this naturally occurs andthus is anyway present in the compounds of formula I.

The compounds of the present invention may be amorphous or may exist inone ore more different crystalline states (polymorphs) which may havedifferent macroscopic properties such as stability or show differentbiological properties such as activities. The present invention includesboth amorphous and crystalline compounds of formula I, their enantiomersor diastereomers, mixtures of different crystalline states of therespective compound of formula I, its enantiomers or diastereomers, aswell as amorphous or crystalline salts thereof.

Salts of the compounds of the present invention are preferablyagriculturally suitable salts. They can be formed in a customary method,e.g. by reacting the compound with an acid if the compound of thepresent invention has a basic functionality or by reacting the compoundwith a suitable base if the compound of the present invention has anacidic functionality.

Useful agriculturally suitable salts are especially the salts of thosecations or the acid addition salts of those acids whose cations andanions, respectively, do not have any adverse effect on the herbicidalaction of the compounds according to the present invention. Suitablecations are in particular the ions of the alkali metals, preferablylithium, sodium and potassium, of the alkaline earth metals, preferablycalcium, magnesium and barium, and of the transition metals, preferablymanganese, copper, zinc and iron, and also ammonium (NH₄ ₊ ) andsubstituted ammonium in which one to four of the hydrogen atoms arereplaced by C₁-C₄-alkyl, C₁-C₄-hydroxyalkyl, C₁-C₄-alkoxy,C₁-C₄-alkoxy-C₁-C₄-alkyl, hydroxy-C₁-C₄-alkoxy-C₁-C₄-alkyl, phenyl orbenzyl. Examples of substituted ammonium ions comprise methylammonium,isopropylammonium, dimethylammonium, diisopropylammonium,trimethylammonium, tetramethylammonium, tetraethylammonium,tetrabutylammonium, 2-hydroxyethylammonium,2-(2-hydroxyethoxy)ethylammonium, bis(2-hydroxyethyl)ammonium,benzyltrimethylammonium and benzl-triethylammonium, furthermorephosphonium ions, sulfonium ions, preferably tri(C₁-C₄-alkyl)sulfonium,and sulfoxonium ions, preferably tri(C₁-C₄-alkyl)sulfoxonium.

Anions of useful acid addition salts are primarily chloride, bromide,fluoride, hydrogensulfate, sulfate, dihydrogenphosphate,hydrogenphosphate, phosphate, nitrate, bicarbonate, carbonate,hexafluorosilicate, hexafluorophosphate, benzoate, and the anions ofC₁-C₄-alkanoic acids, preferably formate, acetate, propionate andbutyrate. They can be formed by reacting compounds of the presentinvention with an acid of the corresponding anion, preferably withhydrochloric acid, hydrobromic acid, sulfuric acid, phosphoric acid ornitric acid.

The term “undesired vegetation” (“weeds”) is understood to include anyvegetation growing in non-crop-areas or at a crop plant site or locus ofseeded and otherwise desired crop, where the vegetation is any plantspecies, including their germinant seeds, emerging seedlings andestablished vegetation, other than the seeded or desired crop (if any).Weeds, in the broadest sense, are plants considered undesirable in aparticular location.

The organic moieties mentioned in the above definitions of the variablesare—like the term halogen—collective terms for individual listings ofthe individual group members. The prefix C_(n)-C_(m) indicates in eachcase the possible number of carbon atoms in the group.

The term “halogen” denotes in each case fluorine, bromine, chlorine oriodine, in particular fluorine, chlorine or bromine.

The term “partially or completely halogenated” will be taken to meanthat 1 or more, e.g. 1, 2, 3, 4 or 5 or all of the hydrogen atoms of agiven radical have been replaced by a halogen atom, in particular byfluorine or chlorine. A partially or completely halogenated radical istermed below also “halo-radical”. For example, partially or completelyhalogenated alkyl is also termed haloalkyl.

The term “alkyl” as used herein (and in the alkyl moieties of othergroups comprising an alkyl group, e.g. alkoxy, alkylcarbonyl,alkoxycarbonyl, alkylthio, alkylsulfonyl and alkoxyalkyl) denotes ineach case a straight-chain or branched alkyl group having usually from 1to 10 carbon atoms, frequently from 1 to 6 carbon atoms, preferably 1 to4 carbon atoms and in particular from 1 to 3 carbon atoms. Examples ofC₁-C₄-alkyl are methyl, ethyl, n-propyl, iso-propyl, n-butyl, 2-butyl(sec-butyl), isobutyl and tert-butyl. Examples for C₁-C₆-alkyl are,apart those mentioned for C₁-C₄-alkyl, n-pentyl, 1-methylbutyl,2-methylbutyl, 3-methylbutyl, 2,2-dimethylpropyl, 1-ethylpropyl,n-hexyl, 1,1-dimethylpropyl, 1,2-dimethylpropyl, 1-methylpentyl,2-methylpentyl, 3-methylpentyl, 4-methylpentyl, 1,1-dimethylbutyl,1,2-dimethylbutyl, 1,3-dimethylbutyl, 2,2-dimethylbutyl,2,3-dimethylbutyl, 3,3-dimethylbutyl, 1-ethylbutyl, 2-ethylbutyl,1,1,2-trimethylpropyl, 1,2,2-trimethylpropyl, 1-ethyl-1-methylpropyl and1-ethyl-2-methylpropyl. Examples for C₁-C₁₀-alkyl are, apart thosementioned for C₁-C₆-alkyl, n-heptyl, 1-methylhexyl, 2-methylhexyl,3-methylhexyl, 4-methylhexyl, 5-methylhexyl, 1-ethylpentyl,2-ethylpentyl, 3-ethylpentyl, n-octyl, 1-methyloctyl, 2-methylheptyl,1-ethylhexyl, 2-ethylhexyl, 1,2-dimethylhexyl, 1-propylpentyl,2-propylpentyl, nonyl, decyl, 2-propylheptyl and 3-propylheptyl.

The term “alkylene” (or alkanediyl) as used herein in each case denotesan alkyl radical as defined above, wherein one hydrogen atom at anyposition of the carbon backbone is replaced by one further binding site,thus forming a bivalent moiety.

The term “haloalkyl” as used herein (and in the haloalkyl moieties ofother groups comprising a haloalkyl group, e.g. haloalkoxy,haloalkylthio, haloalkylcarbonyl, haloalkylsulfonyl andhaloalkylsulfinyl) denotes in each case a straight-chain or branchedalkyl group having usually from 1 to 8 carbon atoms (“C₁-C₈-haloalkyl”),frequently from 1 to 6 carbon atoms (“C₁-C₆-haloalkyl”), more frequently1 to 4 carbon atoms (“C₁-C₄-haloalkyl”), wherein the hydrogen atoms ofthis group are partially or totally replaced with halogen atoms.Preferred haloalkyl moieties are selected from C₁-C₄-haloalkyl, morepreferably from C₁-C₂-haloalkyl, more preferably from halomethyl, inparticular from C₁-C₂-fluoroalkyl. Halomethyl is methyl in which 1, 2 or3 of the hydrogen atoms are replaced by halogen atoms. Examples arebromomethyl, chloromethyl, dichloromethyl, trichloromethyl,fluoromethyl, difluoromethyl, trifluoromethyl, chlorofluoromethyl,dichlorofluoromethyl, chlorodifluoromethyl and the like. Examples forC₁-C₂-fluoroalkyl are fluoromethyl, difluoromethyl, trifluoromethyl,1-fluoroethyl, 2-fluoroethyl, 2,2-difluoroethyl, 2,2,2-trifluoroethyl,pentafluoroethyl, and the like. Examples for C₁-C₂-haloalkyl are, apartthose mentioned for C₁-C₂-fluoroalkyl, chloromethyl, dichloromethyl,trichloromethyl, bromomethyl, chlorofluoromethyl, dichlorofluoromethyl,chlorodifluoromethyl, 1-chloroethyl, 2-chloroethyl, 2,2,-dichloroethyl,2,2,2-trichloroethyl, 2-chloro-2-fluoroethyl,2-chloro-2,2-difluoroethyl, 2,2-dichloro-2-fluoroethyl, 1-bromoethyl,and the like. Examples for C₁-C₄-haloalkyl are, apart those mentionedfor C₁-C₂-haloalkyl, 1-fluoropropyl, 2-fluoropropyl, 3-fluoropropyl,3,3-difluoropropyl, 3,3,3-trifluoropropyl, heptafluoropropyl,1,1,1-trifluoroprop-2-yl, 3-chloropropyl, 4-chlorobutyl and the like.

The term “cycloalkyl” as used herein (and in the cycloalkyl moieties ofother groups comprising a cycloalkyl group, e.g. cycloalkoxy andcycloalkylalkyl) denotes in each case a mono- or bicyclic cycloaliphaticradical having usually from 3 to 10 carbon atoms (“C₃-C₁₀-cycloalkyl”),preferably 3 to 7 carbon atoms (“C₃-C₇-cycloalkyl”) or in particular 3to 6 carbon atoms (“C₃-C₆-cycloalkyl”). Examples of monocyclic radicalshaving 3 to 6 carbon atoms comprise cyclopropyl, cyclobutyl, cyclopentyland cyclohexyl. Examples of monocyclic radicals having 3 to 7 carbonatoms comprise cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl andcycloheptyl. Examples of bicyclic radicals having 7 or 8 carbon atomscomprise bicyclo[2.1.1]hexyl, bicyclo[2.2.1]heptyl,bicyclo[3.1.1]heptyl, bicyclo[2.2.1]heptyl, bicyclo[2.2.2]octyl andbicyclo[3.2.1]octyl.

The term “halocycloalkyl” as used herein (and in the halocycloalkylmoieties of other groups comprising an halocycloalkyl group, e.g.halocycloalkylmethyl) denotes in each case a mono- or bicycliccycloaliphatic radical having usually from 3 to 10 carbon atoms,preferably 3 to 7 carbon atoms or in particular 3 to 6 carbon atoms,wherein at least one, e.g. 1, 2, 3, 4 or 5 of the hydrogen atoms arereplaced by halogen, in particular by fluorine or chlorine. Examples are1- and 2-fluorocyclopropyl, 1,2-, 2,2- and 2,3-difluorocyclopropyl,1,2,2-trifluorocyclopropyl, 2,2,3,3-tetrafluorocyclpropyl, 1- and2-chlorocyclopropyl, 1,2-, 2,2- and 2,3-dichlorocyclopropyl,1,2,2-trichlorocyclopropyl, 2,2,3,3-tetrachlorocyclpropyl, 1-, 2- and3-fluorocyclopentyl, 1,2-, 2,2-, 2,3-, 3,3-, 3,4-,2,5-difluorocyclopentyl, 1-, 2- and 3-chlorocyclopentyl, 1,2-, 2,2-,2,3-, 3,3-, 3,4-, 2,5-dichlorocyclopentyl and the like.

The term “cycloalkyl-alkyl” used herein denotes a cycloalkyl group, asdefined above, which is bound to the remainder of the molecule via analkylene group. The term “C₃-C₇-cycloalkyl-C₁-C₄-alkyl” refers to aC₃-C₇-cycloalkyl group as defined above which is bound to the remainderof the molecule via a C₁-C₄-alkyl group, as defined above. Examples arecyclo-propylmethyl, cyclopropylethyl, cyclopropylpropyl,cyclobutylmethyl, cyclobutylethyl, cyclobu-tylpropyl, cyclopentylmethyl,cyclopentylethyl, cyclopentylpropyl, cyclohexylmethyl, cyclo-hexylethyl,cyclohexylpropyl, and the like.

The term “alkenyl” as used herein denotes in each case a monounsaturatedstraight-chain or branched hydrocarbon radical having usually 2 to 8(“C₂-C₈-alkenyl”), preferably 2 to 6 carbon atoms (“C₂-C₆-alkenyl”), inparticular 2 to 4 carbon atoms (“C₂-C₄-alkenyl”), and a double bond inany position, for example C₂-C₄-alkenyl, such as ethenyl, 1-propenyl,2-propenyl, 1-methylethenyl, 1-butenyl, 2-butenyl, 3-butenyl,1-methyl-1-propenyl, 2-methyl-1-propenyl, 1-methyl-2-propenyl or2-methyl-2-propenyl; C₂-C₆-alkenyl, such as ethenyl, 1-propenyl,2-propenyl, 1-methylethenyl, 1-butenyl, 2-butenyl, 3-butenyl,1-methyl-1-propenyl, 2-methyl-1-propenyl, 1-methyl-2-propenyl,2-methyl-2-propenyl, 1-pentenyl, 2-pentenyl, 3-pentenyl, 4-pentenyl,1-methyl-1-butenyl, 2-methyl-1-butenyl, 3-methyl-1-butenyl,1-methyl-2-butenyl, 2-methyl-2-butenyl, 3-methyl-2-butenyl,1-methyl-3-butenyl, 2-methyl-3-butenyl, 3-methyl-3-butenyl,1,1-dimethyl-2-propenyl, 1,2-dimethyl-1-propenyl,1,2-dimethyl-2-propenyl, 1-ethyl-1-propenyl, 1-ethyl-2-propenyl,1-hexenyl, 2-hexenyl, 3-hexenyl, 4-hexenyl, 5-hexenyl,1-methyl-1-pentenyl, 2-methyl-1-pentenyl, 3-methyl-1-pentenyl,4-methyl-1-pentenyl, 1-methyl-2-pentenyl, 2-methyl-2-pentenyl,3-methyl-2-pentenyl, 4-methyl-2-pentenyl, 1-methyl-3-pentenyl,2-methyl-3-pentenyl, 3-methyl-3-pentenyl, 4-methyl-3-pentenyl,1-methyl-4-pentenyl, 2-methyl-4-pentenyl, 3-methyl-4-pentenyl,4-methyl-4-pentenyl, 1,1-dimethyl-2-butenyl, 1,1-dimethyl-3-butenyl,1,2-dimethyl-1-butenyl, 1,2-dimethyl-2-butenyl, 1,2-dimethyl-3-butenyl,1,3-dimethyl-1-butenyl, 1,3-dimethyl-2-butenyl, 1,3-dimethyl-3-butenyl,2,2-dimethyl-3-butenyl, 2,3-dimethyl-1-butenyl, 2,3-dimethyl-2-butenyl,2,3-dimethyl-3-butenyl, 3,3-dimethyl-1-butenyl, 3,3-dimethyl-2-butenyl,1-ethyl-1-butenyl, 1-ethyl-2-butenyl, 1-ethyl-3-butenyl,2-ethyl-1-butenyl, 2-ethyl-2-butenyl, 2-ethyl-3-butenyl,1,1,2-trimethyl-2-propenyl, 1-ethyl-1-methyl-2-propenyl,1-ethyl-2-methyl-1-propenyl, 1-ethyl-2-methyl-2-propenyl and the like,or C₂-C₈-alkenyl, such as the radicals mentioned for C₂-C₆-alkenyl andadditionally 1-heptenyl, 2-heptenyl, 3-heptenyl, 1-octenyl, 2-octenyl,3-octenyl, 4-octenyl and the positional isomers thereof.

The term “haloalkenyl” as used herein, which may also be expressed as“alkenyl which is substituted by halogen”, and the haloalkenyl moietiesin haloalkenyloxy and the like refers to unsaturated straight-chain orbranched hydrocarbon radicals having 2 to 8 (“C₂-C₈-haloalkenyl”) or 2to 6 (“C₂-C₆-haloalkenyl”) or 2 to 4 (“C₂-C₄-haloalkenyl”) carbon atomsand a double bond in any position, where some or all of the hydrogenatoms in these groups are replaced by halogen atoms as mentioned above,in particular fluorine, chlorine and bromine, for example chlorovinyl,chloroallyl and the like.

The term “alkynyl” as used herein denotes unsaturated straight-chain orbranched hydrocarbon radicals having usually 2 to 8 (“C₂-C₈-alkynyl”),frequently 2 to 6 (“C₂-C₆-alkynyl”), preferably 2 to 4 carbon atoms(“C₂-C₄-alkynyl”) and a triple bond in any position, for exampleC₂-C₄-alkynyl, such as ethynyl, 1-propynyl, 2-propynyl, 1-butynyl,2-butynyl, 3-butynyl, 1-methyl-2-propynyl and the like, C₂-C₆-alkynyl,such as ethynyl, 1-propynyl, 2-propynyl, 1-butynyl, 2-butynyl,3-butynyl, 1-methyl-2-propynyl, 1-pentynyl, 2-pentynyl, 3-pentynyl,4-pentynyl, 1-methyl-2-butynyl, 1-methyl-3-butynyl, 2-methyl-3-butynyl,3-methyl-1-butynyl, 1,1-dimethyl-2-propynyl, 1-ethyl-2-propynyl,1-hexynyl, 2-hexynyl, 3-hexynyl, 4-hexynyl, 5-hexynyl,1-methyl-2-pentynyl, 1-methyl-3-pentynyl, 1-methyl-4-pentynyl,2-methyl-3-pentynyl, 2-methyl-4-pentynyl, 3-methyl-1-pentynyl,3-methyl-4-pentynyl, 4-methyl-1-pentynyl, 4-methyl-2-pentynyl,1,1-dimethyl-2-butynyl, 1,1-dimethyl-3-butynyl, 1,2-dimethyl-3-butynyl,2,2-dimethyl-3-butynyl, 3,3-dimethyl-1-butynyl, 1-ethyl-2-butynyl,1-ethyl-3-butynyl, 2-ethyl-3-butynyl, 1-ethyl-1-methyl-2-propynyl andthe like.

The term “haloalkynyl” as used herein, which is also expressed as“alkynyl which is substituted by halogen”, refers to unsaturatedstraight-chain or branched hydrocarbon radicals having usually 2 to 8carbon atoms (“C₂-C₈-haloalkynyl”), frequently 2 to 6(“C₂-C₆-haloalkynyl”), preferably 2 to 4 carbon atoms(“C₂-C₄-haloalkynyl”), and a triple bond in any position (as mentionedabove), where some or all of the hydrogen atoms in these groups arereplaced by halogen atoms as mentioned above, in particular fluorine,chlorine and bromine.

The term “alkoxy” as used herein denotes in each case a straight-chainor branched alkyl group usually having from 1 to 8 carbon atoms(“C₁-C₆-alkoxy”), frequently from 1 to 6 carbon atoms (“C₁-C₆-alkoxy”),preferably 1 to 4 carbon atoms (“C₁-C₄-alkoxy”), which is bound to theremainder of the molecule via an oxygen atom. C₁-C₂-Alkoxy is methoxy orethoxy. C₁-C₄-Alkoxy is additionally, for example, n-propoxy,1-methylethoxy (isopropoxy), butoxy, 1-methylpropoxy (sec-butoxy),2-methylpropoxy (isobutoxy) or 1,1-dimethylethoxy (tert-butoxy).

C₁-C₆-Alkoxy is additionally, for example, pentoxy, 1-methylbutoxy,2-methylbutoxy, 3-methylbutoxy, 1,1-dimethylpropoxy,1,2-dimethylpropoxy, 2,2-dimethylpropoxy, 1-ethylpropoxy, hexoxy,1-methylpentoxy, 2-methylpentoxy, 3-methylpentoxy, 4-methylpentoxy,1,1-dimethylbutoxy, 1,2-dimethylbutoxy, 1,3-dimethylbutoxy,2,2-dimethylbutoxy, 2,3-dimethylbutoxy, 3,3-dimethylbutoxy,1-ethylbutoxy, 2-ethylbutoxy, 1,1,2-trimethylpropoxy,1,2,2-trimethylpropoxy, 1-ethyl-1-methylpropoxy or1-ethyl-2-methylpropoxy. C₁-C₈-Alkoxy is additionally, for example,heptyloxy, octyloxy, 2-ethylhexyloxy and positional isomers thereof.

The term “haloalkoxy” as used herein denotes in each case astraight-chain or branched alkoxy group, as defined above, having from 1to 8 carbon atoms (“C₁-C₈-haloalkoxy”), frequently from 1 to 6 carbonatoms (“C₁-C₆-haloalkoxy”), preferably 1 to 4 carbon atoms(“C₁-C₄-haloalkoxy”), more preferably 1 to 3 carbon atoms(“C₁-C₃-haloalkoxy”), wherein the hydrogen atoms of this group arepartially or totally replaced with halogen atoms, in particular fluorineatoms. C₁-C₂-Haloalkoxy is, for example, OCH₂F, OCHF₂, OCF₃, OCH₂Cl,OCHCl₂, OCCl₃, chlorofluoromethoxy, dichlorofluoromethoxy,chlorodifluoromethoxy, 2-fluoroethoxy, 2-chloroethoxy, 2-bromoethoxy,2-iodoethoxy, 2,2-difluoroethoxy, 2,2,2-trifluoroethoxy,2-chloro-2-fluoroethoxy, 2-chloro-2,2-difluoroethoxy,2,2-dichloro-2-fluoroethoxy, 2,2,2-trichloroethoxy or OC₂F₅.C₁-C₄-Haloalkoxy is additionally, for example, 2-fluoropropoxy,3-fluoropropoxy, 2,2-difluoropropoxy, 2,3-difluoropropoxy,2-chloropropoxy, 3-chloropropoxy, 2,3-dichloropropoxy, 2-bromopropoxy,3-bromopropoxy, 3,3,3-trifluoropropoxy, 3,3,3-trichloropropoxy,OCH₂—C₂F₅, OCF₂—C₂F₅, 1-(CH₂F)-2-fluoroethoxy, 1-(CH₂Cl)-2-chloroethoxy,1-(CH₂Br)-2-bromoethoxy, 4-fluorobutoxy, 4-chlorobutoxy, 4-bromobutoxyor nonafluorobutoxy. C₁-C₆-Haloalkoxy is additionally, for example,5-fluoropentoxy, 5-chloropentoxy, 5-brompentoxy, 5-iodopentoxy,unde-cafluoropentoxy, 6-fluorohexoxy, 6-chlorohexoxy, 6-bromohexoxy,6-iodohexoxy or dodecafluo-rohexoxy.

The term “alkoxyalkyl” as used herein denotes in each case alkyl usuallycomprising 1 to 6 carbon atoms, preferably 1 to 4 carbon atoms, wherein1 carbon atom carries an alkoxy radical usually comprising 1 to 8,frequently 1 to 6, in particular 1 to 4, carbon atoms as defined above.“C₁-C₆-alkoxy-C₁-C₆-alkyl” is a C₁-C₆-alkyl group, as defined above, inwhich one hydrogen atom is replaced by a C₁-C₆-alkoxy group, as definedabove. Examples are CH₂OCH₃, CH₂—OC₂H₅, n-propoxymethyl, CH₂—OCH(CH₃)₂,n-butoxymethyl, (1-methylpropoxy)-methyl, (2-methylpropoxy)methyl,CH₂—OC(CH₃)₃, 2-(methoxy)ethyl, 2-(ethoxy)ethyl, 2-(n-propoxy)-ethyl,2-(1-methylethoxy)-ethyl, 2-(n-butoxy)ethyl, 2-(1-methylpropoxy)-ethyl,2-(2-methylpropoxy)-ethyl, 2-(1,1-dimethylethoxy)-ethyl,2-(methoxy)-propyl, 2-(ethoxy)-propyl, 2-(n-propoxy)-propyl,2-(1-methylethoxy)-propyl, 2-(n-butoxy)-propyl,2-(1-methylpropoxy)-propyl, 2-(2-methylpropoxy)-propyl,2-(1,1-dimethylethoxy)-propyl, 3-(methoxy)-propyl, 3-(ethoxy)-propyl,3-(n-propoxy)-propyl, 3-(1-methylethoxy)-propyl, 3-(n-butoxy)-propyl,3-(1-methylpropoxy)-propyl, 3-(2-methylpropoxy)-propyl,3-(1,1-dimethylethoxy)-propyl, 2-(methoxy)-butyl, 2-(ethoxy)-butyl,2-(n-propoxy)-butyl, 2-(1-methylethoxy)-butyl, 2-(n-butoxy)-butyl,2-(1-methylpropoxy)-butyl, 2-(2-methyl-propoxy)-butyl,2-(1,1-dimethylethoxy)-butyl, 3-(methoxy)-butyl, 3-(ethoxy)-butyl,3-(n-propoxy)-butyl, 3-(1-methylethoxy)-butyl, 3-(n-butoxy)-butyl,3-(1-methylpropoxy)-butyl, 3-(2-methylpropoxy)-butyl,3-(1,1-dimethylethoxy)-butyl, 4-(methoxy)-butyl, 4-(ethoxy)-butyl,4-(n-propoxy)-butyl, 4-(1-methylethoxy)-butyl, 4-(n-butoxy)-butyl,4-(1-methylpropoxy)-butyl, 4-(2-methylpropoxy)-butyl,4-(1,1-dimethylethoxy)-butyl and the like.

The term “haloalkoxy-alkyl” as used herein denotes in each case alkyl asdefined above, usually comprising 1 to 6 carbon atoms, preferably 1 to 4carbon atoms, wherein 1 carbon atom carries an haloalkoxy radical asdefined above, usually comprising 1 to 8, frequently 1 to 6, inparticular 1 to 4, carbon atoms as defined above. Examples arefluoromethoxymethyl, difluoro-methoxymethyl, trifluoromethoxymethyl,1-fluoroethoxymethyl, 2-fluoroethoxymethyl, 1,1-difluoroethoxymethyl,1,2-difluoroethoxymethyl, 2,2-difluoroethoxymethyl,1,1,2-trifluoroethoxymethyl, 1,2,2-trifluoroethoxymethyl,2,2,2-trifluoroethoxymethyl, pentafluoroethox-ymethyl,1-fluoroethoxy-1-ethyl, 2-fluoroethoxy-1-ethyl,1,1-difluoroethoxy-1-ethyl, 1,2-difluoroethoxy-1-ethyl,2,2-difluoroethoxy-1-ethyl, 1,1,2-trifluoroethoxy-1-ethyl,1,2,2-trifluoroethoxy-1-ethyl, 2,2,2-trifluoroethoxy-1-ethyl,pentafluoroethoxy-1-ethyl, 1-fluoroethoxy-2-ethyl,2-fluoroethoxy-2-ethyl, 1,1-difluoroethoxy-2-ethyl,1,2-difluoroethoxy-2-ethyl, 2,2-difluoroethoxy-2-ethyl,1,1,2-trifluoroethoxy-2-ethyl, 1,2,2-trifluoroethoxy-2-ethyl,2,2,2-trifluoroethoxy-2-ethyl, pentafluoroethoxy-2-ethyl, and the like.

The term “alkylthio” (also alkylsulfanyl, “alkyl-S” or “alkyl-S(O)_(k)”(wherein k is 0)) as used herein denotes in each case a straight-chainor branched saturated alkyl group as defined above, usually comprising 1to 8 carbon atoms (“C₁-C₈-alkylthio”), frequently comprising 1 to 6carbon atoms (“C₁-C₆-alkylthio”), preferably 1 to 4 carbon atoms(“C₁-C₄-alkylthio”), which is attached via a sulfur atom at any positionin the alkyl group. C₁-C₂-Alkylthio is methylthio or ethylthio.C₁-C₄-Alkylthio is additionally, for example, n-propylthio,1-methylethylthio (iso-propylthio), butylthio, 1-methylpropylthio(sec-butylthio), 2-methylpropylthio (isobutylthio) or1,1-dimethylethylthio (tert-butylthio). C₁-C₆-Alkylthio is additionally,for example, pentylthio, 1-methylbutylthio, 2-methylbutylthio,3-methylbutylthio, 1,1-dimethylpropylthio, 1,2-dimethylpropylthio,2,2-dimethylpropylthio, 1-ethylpropylthio, hexylthio,1-methylpentylthio, 2-methylpentylthio, 3-methylpentylthio,4-methylpentylthio, 1,1-dimethylbutylthio, 1,2-dimethylbutylthio,1,3-dimethylbutylthio, 2,2-dimethylbutylthio, 2,3-dimethylbutylthio,3,3-dimethylbutylthio, 1-ethylbutylthio, 2-ethylbutylthio,1,1,2-trimethylpropylthio, 1,2,2-trimethylpropylthio,1-ethyl-1-methylpropylthio or 1-ethyl-2-methylpropylthio.C₁-C₈-Alkylthio is additionally, for example, heptylthio, octylthio,2-ethylhexylthio and positional isomers thereof.

The term “haloalkylthio” as used herein refers to an alkylthio group asdefined above wherein the hydrogen atoms are partially or completelysubstituted by fluorine, chlorine, bromine and/or iodine.C₁-C₂-Haloalkylthio is, for example, SCH₂F, SCHF₂, SCF₃, SCH₂Cl, SCHCl₂,SCCl₃, chlorofluoromethylthio, dichlorofluoromethylthio,chlorodifluoromethylthio, 2-fluoroethylthio, 2-chloroethylthio,2-bromoethylthio, 2-iodoethylthio, 2,2-difluoroethylthio,2,2,2-trifluoroethylthio, 2-chloro-2-fluoroethylthio,2-chloro-2,2-difluoroethylthio, 2,2-dichloro-2-fluoroethylthio,2,2,2-trichloroethylthio or SC₂F₅. C₁-C₄-Haloalkylthio is additionally,for example, 2-fluoropropylthio, 3-fluoropropylthio,2,2-difluoropropylthio, 2,3-difluoropropylthio, 2-chloropropylthio,3-chloropropylthio, 2,3-dichloropropylthio, 2-bromopropylthio,3-bromopropylthio, 3,3,3-trifluoropropylthio, 3,3,3-trichloropropylthio,SCH₂—C₂F₅, SCF₂—C₂F₅, 1-(CH₂F)-2-fluoroethylthio,1-(CH₂Cl)-2-chloroethylthio, 1-(CH₂Br)-2-bromoethylthio,4-fluorobutylthio, 4-chlorobutylthio, 4-bromobutylthio ornonafluorobutylthio. C₁-C₆-Haloalkylthio is additionally, for example,5-fluoropentylthio, 5-chloropentylthio, 5-brompentylthio,5-iodopentylthio, undecafluoropentylthio, 6-fluorohexylthio,6-chlorohexylthio, 6-bromohexylthio, 6-iodohexylthio ordodecafluorohexylthio.

The terms “alkylsulfinyl” and “alkyl-S(O)_(k)” (wherein k is 1) areequivalent and, as used herein, denote an alkyl group, as defined above,attached via a sulfinyl [S(O)] group. For example, the term“C₁-C₂-alkylsulfinyl” refers to a C₁-C₂-alkyl group, as defined above,attached via a sulfinyl [S(O)] group. The term “C₁-C₄-alkylsulfinyl”refers to a C₁-C₄-alkyl group, as defined above, attached via a sulfinyl[S(O)] group. The term “C₁-C₆-alkylsulfinyl” refers to a C₁-C₆-alkylgroup, as defined above, attached via a sulfinyl [S(O)] group.C₁-C₂-alkylsulfinyl is methylsulfinyl or ethylsulfinyl.C₁-C₄-alkylsulfinyl is additionally, for example, n-propylsulfinyl,1-methylethylsulfinyl (isopropylsulfinyl), butylsulfinyl,1-methylpropylsulfinyl (sec-butylsulfinyl), 2-methylpropylsulfinyl(isobutylsulfinyl) or 1,1-dimethylethylsulfinyl (tert-butylsulfinyl).C₁-C₆-alkylsulfinyl is additionally, for example, pentylsulfinyl,1-methylbutylsulfinyl, 2-methylbutylsulfinyl, 3-methylbutylsulfinyl,1,1-dimethylpropylsulfinyl, 1,2-dimethylpropylsulfinyl,2,2-dimethylpropylsulfinyl, 1-ethylpropylsulfinyl, hexylsulfinyl,1-methylpentylsulfinyl, 2-methylpentylsuIfinyl, 3-methylpentylsulfinyl,4-methylpentylsulfinyl, 1,1-dimethylbutylsulfinyl,1,2-dimethylbutylsulfinyl, 1,3-dimethylbutylsulfinyl,2,2-dimethylbutylsulfinyl, 2,3-dimethylbutylsulfinyl,3,3-dimethylbutylsulfinyl, 1-ethylbutylsulfinyl, 2-ethylbutylsulfinyl,1,1,2-trimethylpropylsulfinyl, 1,2,2-trimethylpropylsulfinyl,1-ethyl-1-methylpropylsulfinyl or 1-ethyl-2-methylpropylsulfinyl.

The terms “alkylsulfonyl” and “alkyl-S(O)_(k)” (wherein k is 2) areequivalent and, as used herein, denote an alkyl group, as defined above,attached via a sulfonyl [S(O)₂] group. The term “C₁-C₂-alkylsulfonyl”refers to a C₁-C₂-alkyl group, as defined above, attached via a sulfonyl[S(O)₂] group. The term “C₁-C₄-alkylsulfonyl” refers to a C₁-C₄-alkylgroup, as defined above, attached via a sulfonyl [S(O)₂] group. The term“C₁-C₆-alkylsulfonyl” refers to a C₁-C₆-alkyl group, as defined above,attached via a sulfonyl [S(O)₂] group. C₁-C₂-alkylsulfonyl ismethylsulfonyl or ethylsulfonyl. C₁-C₄-alkylsulfonyl is additionally,for example, n-propylsulfonyl, 1-methylethylsulfonyl(isopropylsulfonyl), butylsulfonyl, 1-methylpropylsulfonyl(sec-butylsulfonyl), 2-methylpropylsulfonyl (isobutylsulfonyl) or1,1-dimethylethylsulfonyl (tert-butylsulfonyl). C₁-C₆-alkylsulfonyl isadditionally, for example, pentylsulfonyl, 1-methylbutylsulfonyl,2-methylbutylsulfonyl, 3-methylbutylsulfonyl,1,1-dimethylpropylsulfonyl, 1,2-dimethylpropylsulfonyl,2,2-dimethylpropylsulfonyl, 1-ethylpropylsulfonyl, hexylsulfonyl,1-methylpentylsulfonyl, 2-methylpentylsulfonyl, 3-methylpentylsulfonyl,4-methylpentylsulfonyl, 1,1-dimethylbutylsulfonyl,1,2-dimethylbutylsulfonyl, 1,3-dimethylbutylsulfonyl,2,2-dimethylbutylsulfonyl, 2,3-dimethylbutylsulfonyl,3,3-dimethylbutylsulfonyl, 1-ethylbutylsulfonyl, 2-ethylbutylsulfonyl,1,1,2-trimethylpropylsulfonyl, 1,2,2-trimethylpropylsulfonyl,1-ethyl-1-methylpropylsulfonyl or 1-ethyl-2-methylpropylsulfonyl.

The term “alkylamino” as used herein denotes in each case a group R*HN—,wherein R* is a straight-chain or branched alkyl group usually havingfrom 1 to 6 carbon atoms (“C₁-C₆-alkylamino”), preferably 1 to 4 carbonatoms (“C₁-C₄-alkylamino”). Examples of C₁-C₆-alkylamino aremethylamino, ethylamino, n-propylamino, isopropylamino, n-butylamino,2-butylamino, iso-butylamino, tert-butylamino, and the like.

The term “dialkylamino” as used herein denotes in each case a groupR*R°N—, wherein R* and R°, independently of each other, are astraight-chain or branched alkyl group each usually having from 1 to 6carbon atoms (“di-(C₁-C₆-alkyl)-amino”), preferably 1 to 4 carbon atoms(“di-(C₁-C₄-alkyl)-amino”). Examples of a di-(C₁-C₆-alkyl)-amino groupare dimethylamino, diethyla-mino, dipropylamino, dibutylamino,methyl-ethyl-amino, methyl-propyl-amino, methyl-isopropylamino,methyl-butyl-amino, methyl-isobutyl-amino, ethyl-propyl-amino,ethyl-isopropylamino, ethyl-butyl-amino, ethyl-isobutyl-amino, and thelike.

The suffix “-carbonyl” in a group denotes in each case that the group isbound to the remainder of the molecule via a carbonyl C═O group. This isthe case e.g. in alkylcarbonyl, haloalkylcarbonyl, aminocarbonyl,alkylaminocarbonyl, dialkylaminocarbonyl, alkoxycarbonyl,haloalkoxycarbonyl.

The term “aryl” as used herein refers to a mono-, bi- or tricyclicaromatic hydrocarbon radical such as phenyl or naphthyl, in particularphenyl.

The term “het(ero)aryl” as used herein refers to a mono-, bi- ortricyclic heteroaromatic hydrocarbon radical, preferably to a monocyclicheteroaromatic radical, such as pyridyl, pyrimidyl and the like.

The term “3-, 4-, 5- or 6-membered monocyclic or 8-, 9- or 10-memberedbicyclic saturated, unsaturated or aromatic heterocycle containing 1, 2,3 or 4 heteroatoms as ring members selected from the groups consistingof N, O and S” as used herein denotes monocyclic or bicyclic radicals,the monocyclic or bicyclic radicals being saturated, unsaturated oraromatic where N can optionally be oxidized, i.e. in the form of anN-oxide, and S can also optionally be oxidized to various oxidationstates, i.e. as SO or SO₂. An unsaturated heterocycle contains at leastone C—C and/or C—N and/or N—N double bond(s). A fully unsaturatedheterocycle contains as many conjugated C—C and/or C—N and/or N—N doublebonds as allowed by the size(s) of the ring(s). An aromatic monocyclicheterocycle is a fully unsaturated 5- or 6-membered monocyclicheterocycle. An aromatic bicyclic heterocycle is an 8-, 9- or10-membered bicyclic heterocycle consisting of a 5- or 6-memberedheteroaromatic ring which is fused to a phenyl ring or to another 5- or6-membered heteroaromatic ring. The heterocycle may be attached to theremainder of the molecule via a carbon ring member or via a nitrogenring member. As a matter of course, the heterocyclic ring contains atleast one carbon ring atom. If the ring contains more than one O ringatom, these are not adjacent.

Examples of a 3-, 4-, 5- or 6-membered monocyclic saturated heterocycleinclude: oxirane-2-yl, aziridine-1-yl, aziridine-2-yl, oxetan-2-yl,azetidine-1-yl, azetidine-2-yl, azetidine-3-yl, thietane-1-yl,thietan-2-yl, thietane-3-yl, tetrahydrofuran-2-yl, tetrahydrofuran-3-yl,tetrahydrothien-2-yl, tetrahydrothien-3-yl, pyrrolidin-1-yl,pyrrolidin-2-yl, pyrrolidin-3-yl, pyrazolidin-1-yl, pyrazolidin-3-yl,pyrazolidin-4-yl, pyrazolidin-5-yl, imidazolidin-1-yl,imidazolidin-2-yl, imidazolidin-4-yl, oxazolidin-2-yl, oxazolidin-3-yl,oxazolidin-4-yl, oxazolidin-5-yl, isoxazolidin-2-yl, isoxazolidin-3-yl,isoxazolidin-4-yl, isoxazolidin-5-yl, thiazolidin-2-yl,thiazolidin-3-yl, thiazolidin-4-yl, thiazolidin-5-yl,isothiazolidin-2-yl, isothiazolidin-3-yl, isothiazolidin-4-yl,isothiazolidin-5-yl, 1,2,4-oxadiazolidin-3-yl, 1,2,4-oxadiazolidin-5-yl,1,2,4-thiadiazolidin-3-yl, 1,2,4-thiadiazolidin-5-yl,1,2,4-triazolidin-3-yl, 1,3,4-oxadiazolidin-2-yl,1,3,4-thiadiazolidin-2-yl, 1,3,4-triazolidin-1-yl,1,3,4-triazolidin-2-yl, 2-tetrahydropyranyl, 4-tetrahydropyranyl,1,3-dioxan-5-yl, 1,4-dioxan-2-yl, piperidin-1-yl, piperidin-2-yl,piperidin-3-yl, piperidin-4-yl, hexahydropyridazin-3-yl,hexahydropyridazin-4-yl, hexahydropyrimidin-2-yl,hexahydropyrimidin-4-yl, hexahydropyrimidin-5-yl, piperazin-1-yl,piperazin-2-yl, 1,3,5-hexahydrotriazin-1-yl, 1,3,5-hexahydrotriazin-2-yland 1,2,4-hexahydrotriazin-3-yl, morpholin-2-yl, morpholin-3-yl,morpholin-4-yl, thiomorpholin-2-yl, thiomorpholin-3-yl,thiomorpholin-4-yl, 1-oxothiomorpholin-2-yl, 1-oxothiomorpholin-3-yl,1-oxothiomorpholin-4-yl, 1,1-dioxothiomorpholin-2-yl,1,1-dioxothiomorpholin-3-yl, 1,1-dioxothiomorpholin-4-yl and the like.

Examples of a 5- or 6-membered monocyclic partially unsaturatedheterocycle include: 2,3-dihydrofur-2-yl, 2,3-dihydrofur-3-yl,2,4-dihydrofur-2-yl, 2,4-dihydrofur-3-yl, 2,3-dihydrothien-2-yl,2,3-dihydrothien-3-yl, 2,4-dihydrothien-2-yl, 2,4-dihydrothien-3-yl,2-pyrrolin-2-yl, 2-pyrrolin-3-yl, 3-pyrrolin-2-yl, 3-pyrrolin-3-yl,2-isoxazolin-3-yl, 3-isoxazolin-3-yl, 4-isoxazolin-3-yl,2-isoxazolin-4-yl, 3-isoxazolin-4-yl, 4-isoxazolin-4-yl,2-isoxazolin-5-yl, 3-isoxazolin-5-yl, 4-isoxazolin-5-yl,2-isothiazolin-3-yl, 3-isothiazolin-3-yl, 4-isothiazolin-3-yl,2-isothiazolin-4-yl, 3-isothiazolin-4-yl, 4-isothiazolin-4-yl,2-isothiazolin-5-yl, 3-isothiazolin-5-yl, 4-isothiazolin-5-yl,2,3-dihydropyrazol-1-yl, 2,3-dihydropyrazol-2-yl,2,3-dihydropyrazol-3-yl, 2,3-dihydropyrazol-4-yl,2,3-dihydropyrazol-5-yl, 3,4-dihydropyrazol-1-yl,3,4-dihydropyrazol-3-yl, 3,4-dihydropyrazol-4-yl,3,4-dihydropyrazol-5-yl, 4,5-dihydropyrazol-1-yl,4,5-dihydropyrazol-3-yl, 4,5-dihydropyrazol-4-yl,4,5-dihydropyrazol-5-yl, 2,3-dihydrooxazol-2-yl, 2,3-dihydrooxazol-3-yl,2,3-dihydrooxazol-4-yl, 2,3-dihydrooxazol-5-yl, 3,4-dihydrooxazol-2-yl,3,4-dihydrooxazol-3-yl, 3,4-dihydrooxazol-4-yl, 3,4-dihydrooxazol-5-yl,3,4-dihydrooxazol-2-yl, 3,4-dihydrooxazol-3-yl, 3,4-dihydrooxazol-4-yl,2-, 3-, 4-, 5- or 6-di- or tetrahydropyridinyl, 3-di- ortetrahydropyridazinyl, 4-di- or tetrahydropyridazinyl, 2-di- ortetrahydropyrimidinyl, 4-di- or tetrahydropyrimidinyl, 5-di- ortetrahydropyrimidinyl, di- or tetrahydropyrazinyl, 1,3,5-di- ortetrahydrotriazin-2-yl and 1,2,4-di- or tetrahydrotriazin-3-yl.

A 5- or 6-membered monocyclic fully unsaturated (including aromatic)heterocyclic ring is e.g. a 5- or 6-membered monocyclic fullyunsaturated (including aromatic) heterocyclic ring. Examples are:2-furyl, 3-furyl, 2-thienyl, 3-thienyl, 1-pyrrolyl, 2-pyrrolyl,3-pyrrolyl, 1-pyrazolyl, 3-pyrazolyl, 4-pyrazolyl, 5-pyrazolyl,2-oxazolyl, 4-oxazolyl, 5-oxazolyl, 2-thiazolyl, 4-thiazolyl,5-thiazolyl, 1-imidazolyl, 2-imidazolyl, 4-imidazolyl,1,3,4-triazol-1-yl, 1,3,4-triazol-2-yl, 2-pyridinyl, 3-pyridinyl,4-pyridinyl, 1-oxopyridin-2-yl, 1-oxopyridin-3-yl, 1-oxopyridin-4-yl,3-pyridazinyl, 4-pyridazinyl, 2-pyrimidinyl, 4-pyrimidinyl,5-pyrimidinyl and 2-pyrazinyl.

Examples of a 5- or 6-membered heteroaromatic ring fused to a phenylring or to a 5- or 6-membered heteroaromatic radical includebenzofuranyl, benzothienyl, indolyl, indazolyl, benzimidazolyl,benzoxathiazolyl, benzoxadiazolyl, benzothiadiazolyl, benzoxazinyl,chinolinyl, isochinolinyl, purinyl, 1,8-naphthyridyl, pteridyl,pyrido[3,2-d]pyrimidyl or pyridoimidazolyl and the like.

If two radicals bound on the same nitrogen atom (for example R^(e) andR^(f) or R^(2e) and R^(2f) or R^(g) and R^(h) or R^(2g) and R^(2h))together with the nitrogen atom, to which they are bound, form a 5-, 6or 7-membered, saturated or unsaturated N-bound heterocyclic radical,which may carry as a ring member a further heteroatom selected from O, Sand N, this is for example pyrrolidine-1-yl, pyrazolidin-1-yl,imidazolidin-1-yl, oxazolidin-3-yl, thiazolidin-3-yl, isoxazolidin-2-yl,isothiazolin-2-yl, [1,2,3]-triazolidin-1-yl, [1,2,3]-triazolidin-2-yl,[1,2,4]-triazolidin-1-yl, [1,2,4]-triazolidin-4-yl,[1,2,3]-oxadiazolidin-2-yl, [1,2,3]-oxadiazolidin-3-yl,[1,2,5]-oxadiazolidin-2-yl, [1,2,4]-oxadiazolidin-2-yl,[1,2,4]-oxadiazolidin-4-yl, [1,3,4]-oxadiazolidin-3-yl,[1,2,3]-thiadiazolidin-2-yl, [1,2,3]-thiadiazolidin-3-yl,[1,2,5]-thiadiazolidin-2-yl, [1,2,4]-thiadiazolidin-2-yl,[1,2,4]-thiadiazolidin-4-yl, [1,3,4]-thiadiazolidin-3-yl, piperdin-1-yl,piperazine-1-yl, morpholin-1-yl, thiomorpholin-1-yl,1-oxothiomorpholin-1-yl, 1,1-dioxothiomorpholin-1-yl, azepan-1-yl,1,4-diazepan-1-yl, pyrrolin-1-yl, pyrazolin-1-yl, imidazolin-1-yl,oxazolin-3-yl, isoxazolin-2-yl, thiazolin-3-yl, isothiazolin-1-yl,1,2-dihydropyridin-1-yl, 1,2,3,4-tetrahydropyridin-1-yl,1,2,5,6-tetrahydropyridin-1-yl, 1,2-dihydropyridazin,1,6-dihydropyridazin, 1,2,3,4-tetrahydropyridazin-1-yl,1,2,5,6-tetrahydropyridazin-1-yl, 1,2-dihydropyrimidin,1,6-dihydropyrimidin, 1,2,3,4-tetrahydropyrimidin-1-yl,1,2,5,6-tetrahydropyrimidin-1-yl, 1,2-dihydropyrazin-1-yl,1,2,3,4-tetrahydropyrazin-1-yl, 1,2,5,6-tetrahydropyrazin-1-yl,pyrrol-1-yl, pyrazol-1-yl, imidazol-1-yl, [1,2,3]-1H-triazol-1-yl,[1,2,3]-2H-triazol-2-yl, [1,2,4]-1H-triazol-1-yl and[1,2,4]-4H-triazol-4-yl.

The remarks made below as to preferred embodiments of the variables(substituents) of the compounds of formula I are valid on their own aswell as preferably in combination with each other, as well as incombination with the stereoisomers, salts, tautomers or N-oxidesthereof.

The remarks made below concerning preferred embodiments of the variablesfurther are valid on their own as well as preferably in combination witheach other concerning the compounds of formulae I, where applicable, aswell as concerning the uses and methods according to the invention andthe composition according to the invention.

Preferred compounds according to the invention are compounds of formulaI or a stereoisomer, salt or N-oxide thereof, wherein the salt is anagriculturally suitable salt. Further preferred compounds according tothe invention are compounds of formula I or an N-oxide or salt thereof,especially an agriculturally suitable salt. Particularly preferredcompounds according to the invention are compounds of formula I or asalt thereof, especially an agriculturally suitable salt thereof.

According to one embodiment of the invention the variable X in thecompounds of formula I is N.

According to another embodiment of the invention the variable X in thecompounds of formula I is CR².

In a preferred embodiment, B is N.

In another preferred embodiment, B is CH.

Preferred compounds according to the invention are compounds of formulaI, wherein R¹ is selected from the group consisting of cyano, halogen,nitro, C₁-C₆-alkyl, C₃-C₆-cycloalkyl, C₂-C₆-alkenyl, C₂-C₆-alkynyl,C₁-C₆-haloalkyl, C₁-C₆-alkoxy, C₁-C₄-alkoxy-C₁-C₄-alkyl,C₁-C₄-haloalkoxy-C₁-C₄-alkyl, C₁-C₄-alkoxy-C₁-C₄-alkoxy-Z¹,C₁-C₄-alkylthio-C₁-C₄-alkyl, C₁-C₄-alkylthio-C₁-C₄-alkylthio-Z¹,C₂-C₆-alkenyloxy, C₂-C₆-alkynyloxy, C₁-C₆-haloalkoxy,C₁-C₄-haloalkoxy-C₁-C₄-alkoxy and R^(1b)—S(O)_(k), where Z¹ is asdefined in claim 1, where k is 0, 1 or 2 and where R^(1b) is selectedfrom C₁-C₄-alkyl and C₁-C₄-haloalkyl.

In a more preferred embodiment, in the compound of formula I, R¹ isselected from the group consisting of halogen, CN, nitro, C₁-C₄-alkyl,C₃-C₆-cycloalkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy-C₁-C₄-alkyl,C₁-C₄-haloalkoxy-C₁-C₄-alkyl, C₁-C₄-alkoxy-C₁-C₄-alkoxy-C₁-C₄-alkyl,C₁-C₄-alkylthio-C₁-C₄-alkyl,C₁-C₄-alkylthio-C₁-C₄-alkylthio-C₁-C₄-alkyl, C₁-C₄-alkoxy,C₁-C₄-haloalkoxy, C₃-C₄-alkenyloxy, C₃-C₄-alkynyloxy,C₁-C₄-alkoxy-C₁-C₄-alkoxy, C₁-C₄-haloalkoxy-C₁-C₄-alkoxy,C₁-C₄-alkyl-S(O)_(k) and C₁-C₄-haloalkyl-S(O)_(k), where k is 0 or 2.

In a highly preferred embodiment, in the compound of formula I, R¹ isselected from the group consisting of halogen, nitro, C₁-C₄-alkyl,C₃-C₆-cycloalkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy-C₁-C₄-alkyl,C₁-C₄-alkoxy-C₁-C₄-alkoxy-C₁-C₄-alkyl, C₁-C₄-alkoxy, C₁-C₄-haloalkoxy,C₁-C₄-alkylthio, C₁-C₄-haloalkylthio and C₁-C₄-alkylsulfonyl.

In one preferred embodiment of the present invention, X as used in thecontext of formula I is N (nitrogen).

In an alternative group of embodiments of the present invention, where Xis CR², the variable R² is hydrogen.

In another group of embodiments of the invention, where X is CR², thevariable R² of the compounds of formula I has any one of the meaningsgiven above for R² with the exception of hydrogen.

According to a preferred embodiment of the invention the variable R² is5- or 6-membered heterocyclyl, where heterocyclyl is a saturated,partially unsaturated or aromatic heterocyclic radical, which containsas a ring member 1 heteroatom selected from the group consisting of O, Nand S and 0, 1, 2 or 3 further nitrogen atoms, where heterocyclyl isunsubstituted or carries 1, 2 or 3 radicals R²¹ which are identical ordifferent.

According to an even more preferred embodiment of the invention, thevariable R² is 5- or 6-membered heterocyclyl selected from the groupconsisting of isoxazolinyl, 1,2-dihydrotetrazolonyl,1,4-dihydrotetrazolonyl, tetrahydrofuryl, dioxolanyl, piperidinyl,morpholinyl, piperazinyl, isoxazolyl, pyrazolyl, thiazolyl, oxazolyl,furyl, pyridinyl, pyrimidinyl and pyrazinyl, where heterocyclyl isunsubstituted or carries 1, 2 or 3 radicals R²¹ which are identical ordifferent and selected from the group consisting of C₁-C₄-alkyl,C₁-C₄-haloalkyl, C₁-C₄-alkoxy, C₁-C₄-alkoxy-C₁-C₄-alkyl andC₁-C₄-alkylthio-C₁-C₄-alkyl.

According to a particular embodiment of the invention the variable R² isselected from the group consisting of hydrogen, halogen, C₁-C₆-alkyl,C₃-C₆-cycloalkyl-C₁-C₄-alkoxy, C₁-C₄-alkoxy-C₁-C₄-alkyl,C₁-C₄-haloalkoxy-C₁-C₄-alkyl, C₂-C₆-alkenyl, C₂-C₆-alkynyl,C₁-C₄-alkoxy, C₁-C₄-haloalkoxy, C₃-C₆-alkenyloxy, C₃-C₆-alkynyloxy,C₃-C₆-haloalkenyloxy, C₃-C₆-haloalkynyloxy, C₁-C₄-alkoxy-C₁-C₄-alkoxy,C₁-C₄-alkoxycarbonyl, C₁-C₄-alkyl-S(O)_(k) and C₁-C₄-haloalkyl-S(O)_(k),where k is 0, 1 or 2, N(C₁-C₄-alkyl)SO₂(C₁-C₄-alkyl), isoxazolyl andisoxazolinyl, where the last two mentioned radicals may be unsubstitutedor carry 1 or 2 radicals selected from halogen and C₁-C₄-alkyl.

In another particular embodiment of the invention, the variable R² informula I is

where

R²⁶ is selected from the group consisting of methyl, ethyl andmethoxyethyl,

R²⁷ is selected from the group consisting of hydrogen, cyano andtrifluoroacetyl,

t is 0 or 1;

or

where

R²⁸ is ethyl and R²⁹ is ethyl, or

R²⁸ and R²⁹ together are —(CH₂)₅— or —(CH₂)₂—O—(CH₂)₂—.

According to a more preferred embodiment of the invention the variableR² in the compounds of formula I is a radical of the following formula:

-   in which # denotes the bond through which the group R² is attached    and:-   R^(P1) is hydrogen or halogen, preferably hydrogen, Cl, Br or F, and    in particular H or F;-   R^(P2) is hydrogen, halogen or C₁-C₂-alkoxy, preferably hydrogen,    Cl, Br, F, OCH₃ or OCH₂CH₃, and in particular H, F, Cl or OCH₃; and-   R^(P3) is hydrogen, halogen, C₁-C₂-alkyl, C₁-C₂-haloalkyl,    C₁-C₂-alkoxy, C₁-C₂-alkoxy-C₁-C₂-alkoxy, preferably hydrogen, Cl,    Br, F, CH₃, C₂H₅, CF₃, CHF₂, CH₂F, CCl₂F, CF₂Cl, CH₂CF₃, CH₂CHF₂,    CF₂CF₃, OCH₃, OCH₂CH₃, OCH₂OCH₃, OCH₂CH₂OCH₂CH₃, OCH₂OCH₂CH₃ or    OCH₂CH₂OCH₃, and in particular is H, F, Cl, CH₃, CF₃, OCH₃, OCH₂CH₃,    OCH₂OCH₃ or OCH₂CH₂OCH₃.

According to a particular embodiment of the invention the variable R² inthe compounds of formula I is phenyl which is unsubstituted or carriesone radical R²¹, where R²¹ is preferably attached to position 4 of thephenyl group and is as defined above and in particular selected fromC₁-C₂-alkyl, C₁-C₂-alkoxy, C₁-C₂-haloalkyl andC₁-C₂-alkoxy-C₁-C₂-alkoxy, preferably form CH₃, C₂H₅, OCH₃, OC₂H₅, CHF₂,CF₃, OCH₂OCH₃ and OCH₂CH₂OCH₃, and specifically from OCH₃ and OC₂H₅.

According to a preferred embodiment of the invention the variable R² inthe compounds of formula I is selected from the group consisting ofhydrogen, halogen, C₁-C₆-alkyl, C₁-C₄-alkoxy-C₁-C₄-alkyl,C₁-C₄-haloalkoxy-C₁-C₄-alkyl, C₂-C₆-alkenyl, C₂-C₆-alkynyl,C₁-C₄-alkoxy, C₁-C₄-haloalkoxy, C₃-C₆-alkenyloxy, C₃-C₆-alkynyloxy,C₃-C₆-haloalkenyloxy, C₃-C₆-haloalkynyloxy, C₁-C₄-alkoxycarbonyl,C₁-C₄-alkyl-S(O)_(k) and C₁-C₄-haloalkyl-S(O)_(k), where k is 0, 1 or 2,isoxazolyl and isoxazolinyl, where the last two mentioned radicals maybe unsubstituted or carry 1 or 2 radicals selected from halogen andC₁-C₄-alkyl.

According to another preferred embodiment of the invention the variableR² in the compounds of formula I is selected from the group consistingof halogen, C₁-C₆-alkyl, C₁-C₄-alkoxy-C₁-C₄-alkyl,C₁-C₄-haloalkoxy-C₁-C₄-alkyl, C₂-C₆-alkenyl, C₂-C₆-alkynyl,C₁-C₄-alkoxy, C₁-C₄-haloalkoxy, C₃-C₆-alkenyloxy, C₃-C₆-alkynyloxy,C₃-C₆-haloalkenyloxy, C₃-C₆-haloalkynyloxy, C₁-C₄-alkoxycarbonyl,C₁-C₄-alkyl-S(O)_(k) and C₁-C₄-haloalkyl-S(O)_(k), where k is 0, 1 or 2,isoxazolyl and isoxazolinyl, where the last two mentioned radicals maybe unsubstituted or carry 1 or 2 radicals selected from halogen andC₁-C₄-alkyl.

According to a more preferred embodiment of the invention the variableR² in the compounds of formula I is selected from C₂-C₄-alkenyl,C₂-C₄-alkynyl, C₁-C₄-alkoxy, C₁-C₂-haloalkoxy-C₁-C₂-alkyl,C₃-C₄-alkenyloxy, C₃-C₄-alkynyloxy, C₁-C₄-alkoxycarbonyl andC₁-C₄-alkyl-S(O₂), and in particular from CH═CH₂, CH═CHCH₃, CH₂OCH₂CF₃,OC₂H₅, OCH₂CH═CH₂, OCH₂C≡CH, C(O)OCH₃, C(O)OC₂H₅, SO₂CH₃, SO₂C₂H₅ andSO₂CH(CH₃)₂.

According to a specifically preferred embodiment of the invention thevariable R² in the compounds of formula I is selected from the groupconsisting of hydrogen, 4,5-dihydroisoxazol-3-yl, which is unsubstitutedor substituted in position 5 with CH₃, CH₂F or CHF₂,4,5-dihydroisoxazol-5-yl, which is unsubstituted or substituted inposition 3 with CH₃, OCH₃, CH₂OCH₃, CH₂SCH₃,1-methyl-5-oxo-1,5-dihydrotetrazol-2-yl,4-methyl-5-oxo-4,5-dihydrotetrazol-1-yl, morpholin-4-yl, isoxazol-3-yl,5-methyl-isoxazol-3-yl, isoxazol-5-yl, 3-methyl-isoxazol-5-yl,1-methyl-1H-pyrazol-3-yl, 2-methyl-2H-pyrazol-3-yl, thiazol-2-yl,4-CH₃-phenyl, 4-C₂H₅-phenyl, 4-OCH₃-phenyl, 4-OC₂H₅-phenyl,4-CHF₂-phenyl, 4-CF₃-phenyl, 4-OCH₂OCH₃-phenyl, 4-OCH₂CH₂OCH₃-phenyl,CH═CH₂, CH═CHCH₃, CH₂OCH₂CF₃, OC₂H₅, OCH₂CH═CH₂, OCH₂C≡CH, C(O)OCH₃,C(O)OC₂H₅, SO₂CH₃, SO₂C₂H₅ and SO₂CH(CH₃)₂, in particular selected fromhydrogen, halogen, methyl, CH₂OCH₂CF₃, methylsulfonyl, ethylsulfonyl,methylsulfanyl, ethylsulfanyl, 3-isoxazolinyl, 5-methyl-3-isoxazolinyl,5-isoxazolinyl, 3-methyl-5-isoxazolinyl, 3-isoxazolyl,5-methyl-3-isoxazolyl, 5-isoxazolyl and 3-methyl-5-isoxazolyl, andspecifically selected from hydrogen, chlorine, methylsulfonyl,methylsulfanyl, CH₂OCH₂CF₃, 3-isoxazolinyl, 5-methyl-3-isoxazolinyl,3-methyl-5-isoxazolinyl, 3-isoxazolyl, 5-methyl-3-isoxazolyl and3-methyl-5-isoxazolyl.

In a highly preferred embodiment, R² is selected from the groupconsisting of hydrogen, halogen, C₁-C₄-alkyl, C₁-C₄-alkoxy,C₁-C₄-haloalkoxy, C₃-C₆-cycloalkyl-C₁-C₂-alkoxy,C₁-C₂-alkoxy-C₁-C₂-alkyl, C₁-C₂-haloalkoxy-C₁-C₂-alkyl,C₁-C₂-alkoxy-C₁-C₂-alkoxy, C₁-C₄-alkyl-S(O)_(k), where k is 0, 1 or 2,N(C₁-C₄-alkyl)SO₂(C₁-C₄-alkyl), isoxazolyl and isoxazolinyl, where thelast two mentioned radicals may be unsubstituted or carry 1 or 2radicals selected from halogen and C₁-C₄-alkyl.

In a particularly preferred embodiment, R² in formula I is selected fromthe group consisting of hydrogen, chlorine, fluorine, methyl, methoxy,ethoxy, OCH₂(cyclo-C₃H₅), OCHF₂, OCH₂CF₃, OCH₂CH₂OCH₃, methoxymethyl,CH₂OCH₂CF₃, methylsulfonyl, ethylsulfonyl, methylsulfinyl,ethylsulfinyl, methylsulfanyl, ethylsulfanyl, NCH₃SO₂CH₃,3-isoxazolinyl, 5-methyl-3-isoxazolinyl, 5-isoxazolinyl,3-methyl-5-isoxazolinyl, 3-isoxazolyl, 5-methyl-3-isoxazolyl,5-isoxazolyl and 3-methyl-5-isoxazolyl, in particular selected from thegroup consisting of hydrogen, chlorine, fluorine, methyl, CH₂OCH₂CF₃,methylsulfonyl, ethylsulfonyl, methylsulfanyl, ethylsulfanyl,3-isoxazolinyl, 5-methyl-3-isoxazolinyl, 5-isoxazolinyl,3-methyl-5-isoxazolinyl, 3-isoxazolyl, 5-methyl-3-isoxazolyl,5-isoxazolyl and 3-methyl-5-isoxazolyl.

Preferred compounds according to the invention are compounds of formulaI, wherein R³ is selected from the group consisting of hydrogen,halogen, cyano, nitro, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy,C₁-C₄-haloalkoxy, C₂-C₄-alkenyl, C₂-C₄-alkynyl, C₃-C₄-alkenyloxy,C₃-C₄-alkynyloxy or R^(2b)—S(O)_(k), where k is 0, 1 or 2 and whereR^(2b) is selected from C₁-C₄-alkyl and C₁-C₄-haloalkyl.

More preferably, R³ is selected from R³ is selected from the groupconsisting of hydrogen, halogen, cyano, nitro, C₁-C₄-alkyl,C₁-C₄-haloalkyl, C₁-C₄-alkoxy, C₁-C₄-haloalkoxy, C₁-C₄-alkylthio,C₁-C₄-haloalkylthio, C₁-C₄-alkyl-S(O)₂ and C₁-C₄-haloalkyl-S(O)₂.

In particular R³ selected from the group consisting of chlorine,fluorine, CF₃, SO₂CH₃, cyano, nitro, hydrogen and CH₃.

Preferred compounds according to the invention are compounds of formulaI, wherein R⁴ is selected from the group consisting of hydrogen, cyano,halogen, nitro, C₁-C₂-alkyl and C₁-C₂-haloalkyl, in particular from thegroup consisting of hydrogen, CHF₂, CF₃, CN, NO₂, CH₃ and halogen, andspecifically from hydrogen, CHF₂, CF₃, CN, NO₂, CH₃, Cl, Br and F.

In particular, R⁴ is selected from the group consisting of hydrogen,CHF₂, CF₃, CN, NO₂, CH₃ and halogen.

Preferred compounds according to the invention are compounds of formulaI, wherein R⁵ is selected from the group consisting of halogen,C₁-C₂-alkyl and C₁-C₂-haloalkyl, and in particular from the groupconsisting of CHF₂, CF₃ and halogen.

According to a particular embodiment of the invention, R⁵ is selectedfrom the group consisting of CHF₂, CF₃ and halogen.

According to a particular embodiment of the invention, R⁴ is hydrogenand R⁵ is chlorine or fluorine.

According to a preferred embodiment of the invention, R⁶ in thecompounds formula I is selected from the group consisting of cyano,C₁-C₆-alkyl, C₁-C₆-cyano-alkyl, C₁-C₆-alkoxy, C₂-C₆-alkenyl,C₂-C₆-haloalkenyl, C₂-C₆-alkynyl, C₂-C₆-haloalkynyl,C₁-C₄-alkoxy-C₁-C₄-alkyl, C₁-C₄-haloalkoxy-C₁-C₄-alkyl,R^(b)R^(b)N—S(O)_(n)—Z, R^(b)O—S(O)_(n)—Z, R^(b)—S(O)_(n)—Z,R^(d)—C(═O)O—C₁-C₃-alkyl, R^(d)—O—C(═O)O—C₁-C₃-alkyl,R^(d)O—C(═O)—C₁-C₃-alkyl, R^(e)R^(f)N—C(═O)—C₁-C₃-alkyl, phenyl-Z andwhere phenyl is unsubstituted or substituted by 1, 2, 3 or 4 groups R′,which are identical or different.

Preferred compounds according to the invention are compounds of formulaI, wherein R⁶ is selected from the group consisting of C₁-C₄-alkyl,C₂-C₆-alkenyl, C₂-C₆-alkynyl, C₁-C₄-alkoxy-C₁-C₄-alkyl,C₃-C₇-cycloalkyl, C₁-C₄-haloalkyl, R^(c)—C(═O)—C₁-C₂-alkyl,R^(d)O—C(═O)—C₁-C₂-alkyl, R^(e)R^(f)N—C(═O)—C₁-C₂-alkyl,R^(k)—C(═O)NH—C₁-C₂-alkyl and benzyl, where

R^(c) is C₁-C₄-alkyl or C₁-C₄-haloalkyl,

R^(d) is C₁-C₄-alkyl,

R^(e) is hydrogen or C₁-C₄-alkyl,

R^(f) is hydrogen or C₁-C₄-alkyl, or

R^(e), R^(f) together with the nitrogen atom, to which they are boundmay form a 5-, 6 or 7-membered, saturated N-bound heterocyclic radical,which may carry as a ring member a further heteroatom selected from O, Sand N and which is unsubstituted or may carry 1, 2, 3 or 4 methylgroups,

R^(k) is C₁-C₄-alkyl.

Further preferred compounds according to the invention are compounds offormula I, wherein R⁶ is selected from the group consisting ofC₁-C₆-alkyl, C₂-C₆-alkenyl, C₂-C₆-alkynyl, C₁-C₄-alkoxy-C₁-C₄-alkyl,R^(d)O—C(═O)—C₁-C₃-alkyl, phenyl-Z and where phenyl is unsubstituted orsubstituted by 1, 2, 3 or 4 groups R′, which are identical or different.

More preferred compounds according to the invention are compounds offormula I, wherein R⁶ is selected from the group consisting of cyano,C₁-C₆-alkyl, C₁-C₆-cyano-alkyl, C₁-C₆-alkoxy, C₂-C₆-alkenyl,C₂-C₆-haloalkenyl, C₂-C₆-alkynyl, C₂-C₆-haloalkynyl,C₁-C₄-alkoxy-C₁-C₄-alkyl, C₁-C₄-haloalkoxy-C₁-C₄-alkyl,R^(b)R^(b)N—S(O)_(n)—Z, R^(b)O—S(O)_(n)—Z, R^(b)—S(O)_(n)—Z,R^(d)—C(═O)O—C₁-C₃-alkyl, R^(d)O—C(═O)—C₁-C₃-alkyl,R^(e)R^(f)N—C(═O)—C₁-C₃-alkyl, phenyl-Z and where phenyl isunsubstituted or substituted by 1, 2, 3 or 4 groups R′, which areidentical or different.

Highly preferably, R⁶ is selected from the group consisting ofC₁-C₆-alkyl, C₂-C₆-alkenyl, C₂-C₆-alkynyl, C₁-C₄-alkoxy-C₁-C₄-alkyl,R^(d)O—C(═O)—C₁-C₃-alkyl, phenyl-Z and where phenyl is unsubstituted orsubstituted by 1, 2, 3 or 4 groups R′, which are identical or different.

Particularly, R6 is selected from the group consisting of methyl, ethyl,methoxymethyl, ethoxymethyl, prop-2-ynyl and methoxycarbonylmethyl;

According to one embodiment, preferred compounds according to theinvention are compounds of formula I, wherein R⁷ is selected from thegroup consisting of hydrogen, C₁-C₄-alkyl, C₂-C₆-alkenyl, C₂-C₆-alkynyl,C₁-C₄-alkoxy-C₁-C₄-alkyl, C₃-C₇-cycloalkyl, C₁-C₄-haloalkyl,R^(c)—C(═O)—C₁-C₂-alkyl, R^(d)O—C(═O)—C₁-C₂-alkyl,R^(e)R^(f)N—C(═O)—C₁-C₂-alkyl, R^(k)—C(═O)NH—C₁-C₂-alkyl and benzyl,where

R^(c) is C₁-C₄-alkyl or C₁-C₄-haloalkyl,

R^(d) is C₁-C₄-alkyl,

R^(e) is hydrogen or C₁-C₄-alkyl,

R^(f) is hydrogen or C₁-C₄-alkyl, or

R^(e), R^(f) together with the nitrogen atom, to which they are boundmay form a 5-, 6 or 7-membered, saturated N-bound heterocyclic radical,which may carry as a ring member a further heteroatom selected from O, Sand N and which is unsubstituted or may carry 1, 2, 3 or 4 methylgroups,

R^(k) is C₁-C₄-alkyl.

According to a highly preferred embodiment, R⁷ is selected from thegroup consisting of C₁-C₄-alkyl, C₃-C₇-cycloalkyl, C₁-C₄-haloalkyl,C₂-C₆-alkenyl, C₂-C₆-alkynyl and C₁-C₄-alkoxy-C₁-C₄-alkyl.

Even more preferably, R⁷ is selected from the group consisting ofmethyl, ethyl, propyl, methoxymethyl, methoxyethyl and ethoxymethyl, inparticular selected from the group consisting of methyl, ethyl andmethoxyethyl.

In this context, the variables R′, R¹¹, R²¹, R²², R²³, R²⁴, R²⁵, R²⁶,R²⁷, R²⁸, Z, Z¹, Z², Z^(2a), R^(a), R^(b), R^(1b), R^(2b), R^(c),R^(2c), R^(d), R^(2d), R^(e), R^(2e), R^(f), R^(2f), R^(g), R^(2g),R^(h), R^(2h), R^(k), n and k, independently of each other, preferablyhave one of the following meanings:

R′, R¹¹, R²¹ independently of each other are selected from halogen,C₁-C₄-alkyl, C₃-C₆-cycloalkyl, C₃-C₆-halocycloalkyl, C₁-C₄-haloalkyl,C₁-C₄-alkoxy, C₁-C₄-alkoxy-C₁-C₄-alkyl, C₁-C₄-alkylthio-C₁-C₄-alkyl,C₁-C₄-alkoxy-C₁-C₄-alkoxy and C₁-C₆-haloalkyloxy, more preferably fromhalogen, C₁-C₄-alkyl, C₃-C₆-cycloalkyl, C₁-C₄-haloalkyl andC₁-C₄-alkoxy.

More preferably R′, R¹¹, R²¹ independently of each other are selectedfrom the group consisting of halogen, C₁-C₄-alkyl, C₃-C₆-cycloalkyl,C₁-C₄-haloalkyl, C₁-C₄-alkoxy, C₁-C₄-alkoxy-C₁-C₄-alkyl,C₁-C₄-alkylthio-C₁-C₄-alkyl and C₁-C₄-alkoxy-C₁-C₄-alkoxy; in particularselected from halogen, C₁-C₄-alkyl, C₁-C₄-alkoxy, C₁-C₄-haloalkyl,C₁-C₄-alkoxy-C₁-C₄-alkyl and C₁-C₄-alkoxy-C₁-C₄-alkoxy; and specificallyfrom Cl, F, Br, methyl, ethyl, methoxy and trifluoromethyl.

R²² is selected from the group consisting of hydrogen, C₁-C₆-alkyl,C₁-C₆-haloalkyl, C₂-C₆-alkenyl, C₂-C₆-haloalkenyl, C₂-C₆-alkynyl,C₃-C₆-haloalkynyl, C₃-C₆-cycloalkyl, C₃-C₆-cycloalkenyl,C₃-C₆-halocycloalkyl, C₃-C₆-cycloalkyl-C₁-C₆-alkyl,C₁-C₆-alkoxy-C₁-C₆-alkyl, C₃-C₆-cycloalkyl-C₁-C₆-alkoxy-C₁-C₆-alkyl,phenyl, phenyl-C₁-C₆-alkyl, heteroaryl, heteroaryl-C₁-C₆-alkyl,heterocyclyl, heterocyclyl-C₁-C₆-alkyl, phenyl-O—C₁-C₆-alkyl,heteroaryl-O—C₁-C₆-alkyl, heterocyclyl-O—C₁-C₆-alkyl,phenyl-N(R²³)—C₁-C₆-alkyl, heteroaryl-N(R²³)—C₁-C₆-alkyl,heterocyclyl-N(R²³)—C₁-C₆-alkyl, phenyl-S(O)_(n)—C₁-C₆-alkyl,heteroaryl-S(O)_(n)—C₁-C₆-alkyl, heterocyclyl-S(O)_(n)—C₁-C₆-alkyl,where the 15 aforementioned radicals are substituted by s residuesselected from the group consisting of nitro, halogen, cyano, rhodano,C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₃-C₆-cycloalkyl, C(O)OR²³, C(O)N(R²³)₂,OR²³, N(R²³)₂, S(O)_(n)R²⁴, S(O)₂OR²³, S(O)₂N(R²³)₂ andR²³O—C₁-C₆-alkyl, and where heterocyclyl bears 0, 1 or 2 oxo groups;

R²³ is selected from the group consisting of hydrogen, C₁-C₆-alkyl,C₁-C₆-haloalkyl, C₂-C₆-alkenyl, C₂-C₆-alkynyl, C₃-C₆-cycloalkyl,C₃-C₆-cycloalkyl-C₁-C₆-alkyl and phenyl;

R²⁴ is selected from the group consisting of C₁-C₆-alkyl,C₁-C₆-haloalkyl, C₂-C₆-alkenyl, C₂-C₆-alkynyl, C₃-C₆-cycloalkyl,C₃-C₆-cycloalkyl-C₁-C₆-alkyl and phenyl;

R²⁵ is selected from the group consisting of C₁-C₆-alkyl,C₁-C₆-haloalkyl, C₂-C₆-alkenyl, C₂-C₆-haloalkenyl, C₂-C₆-alkynyl,C₃-C₆-haloalkynyl, C₃-C₆-cycloalkyl, C₃-C₆-cycloalkenyl,C₃-C₆-halocycloalkyl, C₃-C₆-cycloalkyl-C₁-C₆-alkyl,C₁-C₆-alkoxy-C₁-C₆-alkyl, C₃-C₆-cycloalkyl-C₁-C₆-alkoxy-C₁-C₆-alkyl,phenyl, phenyl-C₁-C₆-alkyl, heteroaryl, heteroaryl-C₁-C₆-alkyl,heterocyclyl, heterocyclyl-C₁-C₆-alkyl, phenyl-O—C₁-C₆-alkyl,heteroaryl-O—C₁-C₆-alkyl, heterocyclyl-O—C₁-C₆-alkyl,phenyl-N(R²³)—C₁-C₆-alkyl, heteroaryl-N(R²³)—C₁-C₆-alkyl,heterocyclyl-N(R²³)—C₁-C₆-alkyl, phenyl-S(O)_(n)—C₁-C₆-alkyl,heteroaryl-S(O)_(n)—C₁-C₆-alkyl, heterocyclyl-S(O)_(n)—C₁-C₆-alkyl,where the 15 aforementioned radicals are substituted by s residuesselected from the group consisting of nitro, halogen, cyano, rhodano,C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₃-C₆-cycloalkyl, C(O)OR²³, C(O)N(R²³)₂,OR²³, N(R²³)₂, S(O)_(n)R²⁴, S(O)₂OR²³, S(O)₂N(R²³)₂ andR²³O—C₁-C₆-alkyl, and where heterocyclyl bears 0, 1 or 2 oxo groups;

R²⁶ is C₁-C₆-alkyl or C₁-C₄-alkoxy-C₁-C₄-alkyl;

R²⁷ is selected from the group consisting of hydrogen, cyano andC₁-C₄-haloalkylcarbonyl;

R²⁸, R²⁹ independently of each other are C₁-C₆-alkyl, or

R²⁸, R²⁹ together with the sulfur atom, to which they are bound may forma 5- or 6-membered saturated ring, which may carry as a ring member 1oxygen atom;

Z, Z¹, Z² independently of each other are selected from a covalent bond,methanediyl and ethanediyl, and in particular are a covalent bond.

Z^(2a) is selected from a covalent bond, C₁-C₂-alkanediyl,O—C₁-C₂-alkanediyl, C₁-C₂-alkanediyl-O andC₁-C₂-alkanediyl-O—C₁-C₂-alkanediyl; more preferably from a covalentbond, methanediyl, ethanediyl, O-methanediyl, O-ethanediyl,methanediyl-O, and ethanediyl-O; and in particular from a covalent bond,methanediyl and ethanediyl.

R^(b), R^(1b), R^(2b) independently of each other are selected fromC₁-C₆-alkyl, C₃-C₇-cycloalkyl, C₁-C₆-haloalkyl, C₂-C₆-alkenyl,C₂-C₆-haloalkenyl, C₂-C₆-alkynyl, C₂-C₆-haloalkynyl, phenyl andheterocyclyl, where heterocyclyl is a 5- or 6-membered monocyclicsaturated, partially unsaturated or aromatic heterocycle, which contains1, 2 or 3 heteroatoms as ring members, which are selected from the groupconsisting of O, N and S, where phenyl and heterocyclyl areunsubstituted or substituted by 1, 2 or 3 groups, which are identical ordifferent and selected from the group consisting of halogen,C₁-C₄-alkyl, C₁-C₂-haloalkyl and C₁-C₂-alkoxy.

More preferably R^(b), R^(1b), R^(2b) independently of each other areselected from the group consisting of C₁-C₄-alkyl, C₂-C₄-alkenyl,C₂-C₄-alkynyl, C₁-C₄-haloalkyl, C₂-C₄-haloalkenyl, C₂-C₄-haloalkynyl,C₃-C₆-cycloalkyl, phenyl and heterocyclyl, where heterocyclyl is a 5- or6-membered monocyclic saturated, partially unsaturated or aromaticheterocycle, which contains 1, 2 or 3 heteroatoms as ring members, whichare selected from the group consisting of O, N and S.

In particular, R^(b), R^(1b), R^(2b) independently of each other areselected from C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₂-C₄-alkenyl,C₂-C₄-haloalkenyl, C₂-C₄-alkynyl, C₃-C₆-cycloalkyl, phenyl andheterocyclyl, where heterocyclyl is a 5- or 6-membered aromaticheterocyclic radical having 1 or 2 nitrogen atoms as ring members.

R^(c), R^(2c), R^(k) independently of each other are selected fromhydrogen, C₁-C₆-alkyl, C₃-C₇-cycloalkyl, which is unsubstituted orpartly or completely halogenated, C₁-C₆-haloalkyl, C₂-C₆-alkenyl,C₂-C₆-haloalkenyl, C₂-C₆-alkynyl, C₂-C₆-haloalkynyl,C₁-C₄-alkoxy-C₁-C₄-alkyl, phenyl, benzyl and heterocyclyl, whereheterocyclyl is a 5- or 6-membered monocyclic saturated, partiallyunsaturated or aromatic heterocycle, which contains 1, 2 or 3heteroatoms as ring members, which are selected from the groupconsisting of O, N and S, where phenyl, benzyl and heterocyclyl areunsubstituted or substituted by 1, 2 or 3 groups, which are identical ordifferent and selected from the group consisting of halogen,C₁-C₄-alkyl, C₁-C₄-haloalkyl and C₁-C₄-alkoxy.

More preferably R^(c), R^(2c), R^(k) independently of each other areselected from hydrogen, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₂—C-alkenyl,C₂—C-haloalkenyl, C₂—C-alkynyl, C₃-C₆-cycloalkyl, phenyl andheterocyclyl, where heterocyclyl is a 5- or 6-membered monocyclicsaturated, partially unsaturated or aromatic heterocycle, which contains1, 2 or 3 heteroatoms as ring members, which are selected from the groupconsisting of O, N and S.

In particular, R^(c), R^(2c), R^(k) independently of each other areselected from hydrogen, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₂-C₄-alkenyl,C₂-C₄-haloalkenyl, C₃-C₆-cycloalkyl, phenyl and heterocyclyl, whereheterocyclyl is a 5- or 6-membered aromatic heterocyclic radical having1 or 2 nitrogen atoms as ring members.

R^(d), R^(2d) independently of each other are selected from C₁-C₆-alkyl,C₃-C₇-cycloalkyl, which is unsubstituted or partly or completelyhalogenated, C₁-C₆-haloalkyl, C₂-C₆-alkenyl, C₂-C₆-haloalkenyl,C₂-C₆-alkynyl, C₂-C₆-haloalkynyl, C₁-C₄-alkoxy-C₁-C₄-alkyl, phenyl andbenzyl.

More preferably R^(d), R^(2d) independently of each other are selectedfrom C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₂-C₆-alkenyl, C₂-C₆-haloalkenyl,C₂-C₆-alkynyl, C₁-C₄-alkoxy-C₁-C₄-alkyl and C₃-C₇-cycloalkyl, which isunsubstituted or partly or completely halogenated, and in particularselected from C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₂-C₄-alkenyl,C₂-C₄-haloalkenyl, C₂-C₄-alkynyl and C₃-C₆-cycloalkyl.

R^(e), R^(f), R^(2e), R^(2f) independently of each other are selectedfrom the group consisting of hydrogen, C₁-C₆-alkyl, C₃-C₇-cycloalkyl,which is unsubstituted or partially or completely halogenated,C₁-C₆-haloalkyl, C₂-C₆-alkenyl, C₂-C₆-haloalkenyl,C₁-C₄-alkoxy-C₁-C₄-alkyl, phenyl and benzyl, where phenyl and benzyl areunsubstituted or substituted by 1, 2 or 3 groups, which are identical ordifferent and selected from the group consisting of halogen,C₁-C₄-alkyl, C₁-C₄-haloalkyl and C₁-C₄-alkoxy, or R^(e) and R^(f) orR^(2e) and R^(2f) together with the nitrogen atom, to which they arebound may form a 5-, 6 or 7-membered, saturated or unsaturated N-boundheterocyclic radical, which may carry as a ring member a furtherheteroatom selected from O, S and N and which is unsubstituted or maycarry 1, 2, 3 or 4 groups, which are identical or different and selectedfrom the group consisting of halogen, C₁-C₄-alkyl, C₁-C₄-haloalkyl andC₁-C₄-alkoxy.

More preferably R^(e), R^(f), R^(2e), R^(2f) independently of each otherare selected from hydrogen, C₁-C₆-alkyl, C₁-C₆-haloalkyl and benzyl, orR^(e) and R^(f) or R^(2e) and R^(2f) together with the nitrogen atom, towhich they are bound may form a 5- or 6-membered, saturated orunsaturated N-bound heterocyclic radical, which may carry as a ringmember a further heteroatom selected from O, S and N and which isunsubstituted or may carry 1, 2 or 3 groups, which are identical ordifferent and selected from the group consisting of halogen, C₁-C₄-alkyland C₁-C₄-haloalkyl.

In particular, R^(e), R^(f), R^(2e), R^(2f) independently of each otherare selected from hydrogen and C₁-C₄-alkyl, or R^(e) and R^(f) or R^(2e)and R^(2f) together with the nitrogen atom, to which they are bound mayform a 5- or 6-membered, saturated N-bound heterocyclic radical, whichmay carry as a ring member a further heteroatom selected from O, S and Nand which is unsubstituted or may carry 1, 2 or 3 methyl groups.

R^(g), R^(2g) independently of each other are selected from hydrogen,C₁-C₆-alkyl, C₃-C₇-cycloalkyl, which is unsubstituted or partly orcompletely halogenated, C₁-C₆-haloalkyl, C₂-C₆-alkenyl,C₂-C₆-haloalkenyl, C₂-C₆-alkynyl, C₂-C₆-haloalkynyl,C₁-C₄-alkoxy-C₁-C₄-alkyl, C₁-C₄-alkylsulfonyl, C₁-C₄-alkylcarbonyl,phenyl and benzyl.

More preferably R^(g), R^(2g) independently of each other are selectedfrom hydrogen, C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₂-C₆-alkenyl,C₂-C₆-haloalkenyl, benzyl, C₁-C₄-alkoxy-C₁-C₄-alkyl andC₃-C₇-cycloalkyl, which is unsubstituted or partly or completelyhalogenated, and in particular selected from hydrogen, C₁-C₄-alkyl,C₁-C₄-haloalkyl, C₂-C₄-alkenyl, C₂-C₄-haloalkenyl, benzyl andC₃-C₆-cycloalkyl.

R^(h), R^(2h) independently of each other are selected from hydrogen,C₁-C₆-alkyl, C₃-C₇-cycloalkyl, which is unsubstituted or partly orcompletely halogenated, C₁-C₆-haloalkyl, C₂-C₆-alkenyl,C₂-C₆-haloalkenyl, C₂-C₆-alkynyl, C₂-C₆-haloalkynyl,C₁-C₄-alkoxy-C₁-C₄-alkyl, C₁-C₄-alkylsulfonyl, C₁-C₄-alkylcarbonyl,phenyl, benzyl and a radical C(═O)—R^(k), where R^(k) is H, C₁-C₄-alkyl,C₁-C₄-haloalkyl or phenyl.

More preferably R^(h), R^(2h) independently of each other are selectedfrom hydrogen, C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₂-C₆-alkenyl,C₂-C₆-haloalkenyl, benzyl, C₁-C₄-alkoxy-C₁-C₄-alkyl andC₃-C₇-cycloalkyl, which is unsubstituted or partly or completelyhalogenated, and in particular selected from hydrogen, C₁-C₄-alkyl,C₁-C₄-haloalkyl, C₂-C₄-alkenyl, C₂-C₄-haloalkenyl, benzyl andC₃-C₆-cycloalkyl; or R^(g) and R^(h) or R^(2g) and R^(2h) together withthe nitrogen atom, to which they are bound may form a 5-, 6 or7-membered, saturated or unsaturated N-bound heterocyclic radical, whichmay carry as a ring member a further heteroatom selected from O, S and Nand which is unsubstituted or may carry 1, 2, 3 or 4 groups, which areidentical or different and selected from the group consisting of ═O,halogen, C₁-C₄-alkyl and C₁-C₄-haloalkyl and C₁-C₄-alkoxy;

more preferably R^(g) and R^(h) or R^(2g) and R^(2h) together with thenitrogen atom, to which they are bound may form a 5- or 6-membered,saturated or unsaturated N-bound heterocyclic radical, which may carryas a ring member a further heteroatom selected from O, S and N and whichis unsubstituted or may carry 1, 2 or 3 groups, which are identical ordifferent and selected from the group consisting of halogen, C₁-C₄-alkyland C₁-C₄-haloalkyl; and in particular, R^(g) and R^(h) or R^(2g) andR^(2h) together with the nitrogen atom, to which they are bound may forma 5- or 6-membered, saturated N-bound heterocyclic radical, which maycarry as a ring member a further heteroatom selected from O, S and N andwhich is unsubstituted or may carry 1, 2 or 3 methyl groups.

n and k independently of each other are 0 or 2, and in particular 2.

s is 0, 1, 2 or 3.

t is 0 or 1.

Particularly preferably, the variables have the following meaning:

R²² is selected from hydrogen, C₁-C₆-alkyl, C₁-C₆-haloalkyl,C₃-C₆-cycloalkyl, C₃-C₆-halocycloalkyl, C₃-C₆-cycloalkyl-C₁-C₆-alkyl,C₁-C₆-alkoxy-C₁-C₆-alkyl, C₃-C₆-cycloalkyl-C₁-C₆-alkoxy-C₁-C₆-alkyl,phenyl, phenyl-C₁-C₆-alkyl, heteroaryl, heteroaryl-C₁-C₆-alkyl,heterocyclyl, heterocyclyl-C₁-C₆-alkyl, phenyl-O—C₁-C₆-alkyl,heteroaryl-O—C₁-C₆-alkyl, heterocyclyl-O—C₁-C₆-alkyl, where the 9aforementioned radicals are substituted by s residues selected from thegroup consisting of nitro, halogen, C₁-C₆-alkyl, C₁-C₆-haloalkyl,C(O)OR²³, C(O)N(R²³)₂, OR²³, N(R²³)₂, S(O)_(n)R²⁴ and R²³O—C₁-C₆-alkyl,and where heterocyclyl bears 0, 1 or 2 oxo groups.

More preferably R²² is selected from hydrogen, C₁-C₄-alkyl,C₁-C₄-haloalkyl, C₁-C₄-alkoxy-C₁-C₄-alkyl, C₃-C₆-cycloalkyl,C₃-C₆-cycloalkyl-C₁-C₂-alkyl, phenyl and phenyl-C₁-C₂-alkyl. Inparticular, R²² is hydrogen or C₁-C₄-alkyl.

R²³ is selected from hydrogen, C₁-C₄-alkyl, C₁-C₄-haloalkyl andC₃-C₆-cycloalkyl. In particular, R²³ is hydrogen or C₁-C₄-alkyl.

R²⁴ is selected from C₁-C₄-alkyl, C₁-C₄-haloalkyl and C₃-C₆-cycloalkyl.In particular, R²⁴ is C₁-C₄-alkyl.

R²⁵ is selected from C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₃-C₆-cycloalkyl,C₃-C₆-halocycloalkyl, C₃-C₆-cycloalkyl-C₁-C₆-alkyl,C₁-C₆-alkoxy-C₁-C₆-alkyl, C₃-C₆-cycloalkyl-C₁-C₆-alkoxy-C₁-C₆-alkyl,phenyl, phenyl-C₁-C₆-alkyl, heteroaryl, heteroaryl-C₁-C₆-alkyl,heterocyclyl, heterocyclyl-C₁-C₆-alkyl, phenyl-O—C₁-C₆-alkyl,heteroaryl-O—C₁-C₆-alkyl, heterocyclyl-O—C₁-C₆-alkyl, where the 9aforementioned radicals are substituted by s residues selected from thegroup consisting of nitro, halogen, C₁-C₆-alkyl, C₁-C₆-haloalkyl,C(O)OR²³, C(O)N(R²³)₂, OR²³, N(R²³)₂, S(O)_(n)R²⁴ and R²³O—C₁-C₆-alkyl,and where heterocyclyl bears 0, 1 or 2 oxo groups.

More preferably R²⁵ is selected from C₁-C₄-alkyl, C₁-C₄-haloalkyl,C₁-C₄-alkoxy-C₁-C₄-alkyl, C₃-C₆-cycloalkyl,C₃-C₆-cycloalkyl-C₁-C₂-alkyl, phenyl and phenyl-C₁-C₂-alkyl. Inparticular, R²⁵ is C₁-C₄-alkyl.

R²⁶ is selected from the group consisting of methyl, ethyl andmethoxyethyl.

R²⁷ is selected from the group consisting of hydrogen, cyano andtrifluoroacetyl.

R²⁸ is ethyl and R²⁹ is ethyl, or R²⁸ and R²⁹ together are —(CH₂)₅—− or—(CH₂)₂—O—(CH₂)₂—.

s is 0, 1, 2 or 3. In one particular embodiment of the invention, s is0. In another particular embodiment of the invention, s is 1, 2 or 3.

t is 0 or 1. In one particular embodiment of the invention, t is 0. Inanother particular embodiment of the invention, t is 1.

According to one embodiment, preferred compounds according to theinvention are compounds of formula I, where

-   R¹ is selected from the group consisting of halogen, nitro,    C₁-C₄-alkyl, C₃-C₆-cycloalkyl, C₁-C₄-haloalkyl,    C₁-C₄-alkoxy-C₁-C₄-alkyl, C₁-C₄-alkoxy-C₁-C₄-alkoxy-C₁-C₄-alkyl,    C₁-C₄-alkoxy, C₁-C₄-haloalkoxy, C₁-C₄-alkylthio, C₁-C₄-haloalkylthio    and C₁-C₄-alkylsulfonyl; and-   R³ is selected from the group consisting of hydrogen, halogen,    cyano, nitro, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy,    C₁-C₄-haloalkoxy, C₁-C₄-alkylthio, C₁-C₄-haloalkylthio and    C₁-C₄-alkylsulfonyl.

According to an even more preferred embodiment, compounds according tothe invention are compounds of formula I, where X is CR² and thevariables R¹, R², R³, R⁴, R⁵, R⁶ and R⁷ have the following meanings:

-   R¹ is selected from the group consisting of halogen, nitro,    cyclopropyl, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy-C₁-C₄-alkyl,    C₁-C₄-alkoxy-C₁-C₄-alkoxy-C₁-C₄-alkyl and C₁-C₄-alkyl-S(O)₂;-   R² is selected from the group consisting of hydrogen, halogen,    C₁-C₄-alkyl, C₁-C₄-alkoxy, C₁-C₄-haloalkoxy,    C₃-C₆-cycloalkyl-C₁-C₂-alkoxy, C₁-C₂-alkoxy-C₁-C₂-alkyl,    C₁-C₂-haloalkoxy-C₁-C₂-alkyl, C₁-C₂-alkoxy-C₁-C₂-alkoxy,    C₁-C₄-alkyl-S(O)_(k), where k is 0, 1 or 2,    N(C₁-C₄-alkyl)SO₂(C₁-C₄-alkyl), isoxazolyl and isoxazolinyl, where    the last two mentioned radicals may be unsubstituted or carry 1 or 2    radicals selected from halogen and C₁-C₄-alkyl;-   R³ is selected from the group consisting of hydrogen, halogen,    cyano, nitro, C₁-C₄-alkyl, C₁-C₄-haloalkyl and C₁-C₄-alkyl-S(O)₂;-   R⁴ is selected from the group consisting of hydrogen, cyano, methyl    and halogen;-   R⁵ is selected from the group consisting of halogen, CHF₂ and CF₃;-   R⁶ is selected from the group consisting of C₁-C₄-alkyl,    C₁-C₂-alkoxy-C₁-C₂-alkyl, C₂-C₄-alkenyl, C₂-C₄-alkynyl,    C₁-C₄-alkoxycarbonyl-C₁-C₄-alkyl and phenyl-C₁-C₂-alkyl;-   R⁷ is selected from the group consisting of C₁-C₄-alkyl and    C₁-C₂-alkoxy-C₁-C₂-alkyl.

In a preferred embodiment, X is CR² and the variables R¹, R², R³, R⁴,R⁵, R⁶ and R⁷ have the following meanings:

-   -   R¹ is selected from the group consisting of chlorine, nitro,        methyl, cyclopropyl, trifluoromethyl, methoxymethyl,        CH₂OCH₂CH₂OCH₃ and methylsulfonyl;

-   R² is selected from the group consisting of hydrogen, chlorine,    fluorine, methyl, methoxy, ethoxy, OCH₂(cyclo-C₃H₅), OCHF₂, OCH₂CF₃,    OCH₂CH₂OCH₃, methoxymethyl, CH₂OCH₂CF₃, methylsulfonyl,    ethylsulfonyl, methylsulfinyl, ethylsulfinyl, methylsulfanyl,    ethylsulfanyl, NCH₃SO₂CH₃, 3-isoxazolinyl, 5-methyl-3-isoxazolinyl,    5-isoxazolinyl, 3-methyl-5-isoxazolinyl, 3-isoxazolyl,    5-methyl-3-isoxazolyl, 5-isoxazolyl and 3-methyl-5-isoxazolyl;

-   R³ is selected from the group consisting of hydrogen, fluorine,    chlorine, bromine, cyano, nitro, methyl, trifluoromethyl and    methylsulfonyl;

-   R⁴ is selected from the group consisting of hydrogen, cyano, methyl,    chlorine and fluorine;

-   R⁵ is selected from the group consisting of chlorine and fluorine;

-   R⁶ is selected from the group consisting of methyl, ethyl,    methoxymethyl, ethoxymethyl, prop-2-enyl, prop-2-ynyl,    methoxycarbonylmethyl and benzyl;

-   R⁷ is selected from the group consisting of methyl, ethyl, propyl,    methoxymethyl, methoxyethyl and ethoxymethyl.

In another preferred embodiment of the present invention, X is N and thevariables R¹, R³, R⁴, R⁵, R⁶ and R⁷ have the following meanings:

-   R¹ is selected from the group consisting of halogen, nitro,    cyclopropyl, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy-C₁-C₄-alkyl,    C₁-C₄-alkoxy-C₁-C₄-alkoxy-C₁-C₄-alkyl and C₁-C₄-alkyl-S(O)₂;-   R³ is selected from the group consisting of hydrogen, halogen,    cyano, nitro, C₁-C₄-alkyl, C₁-C₄-haloalkyl and C₁-C₄-alkyl-S(O)₂;-   R⁴ is selected from the group consisting of hydrogen, cyano, methyl    and halogen;-   R⁵ is selected from the group consisting of halogen, CHF₂ and CF₃;-   R⁶ is selected from the group consisting of C₁-C₄-alkyl,    C₁-C₂-alkoxy-C₁-C₂-alkyl, C₂-C₄-alkenyl, C₂-C₄-alkynyl,    C₁-C₄-alkoxycarbonyl-C₁-C₄-alkyl and phenyl-C₁-C₂-alkyl;-   R⁷ is selected from the group consisting of C₁-C₄-alkyl and    C₁-C₂-alkoxy-C₁-C₂-alkyl.

In a more preferred embodiment of the present invention, X is N and thevariables R¹, R³, R⁴, R⁵, R⁶ and R⁷ have the following meanings:

-   R¹ is selected from the group consisting of chlorine, nitro, methyl,    cyclopropyl, trifluoromethyl, methoxymethyl, CH₂OCH₂CH₂OCH₃ and    methylsulfonyl;-   R³ is selected from the group consisting of hydrogen, fluorine,    chlorine, bromine, cyano, nitro, methyl, trifluoromethyl and    methylsulfonyl;-   R⁴ is selected from the group consisting of hydrogen, cyano, methyl,    chlorine and fluorine;-   R⁵ is selected from the group consisting of chlorine and fluorine;-   R⁶ is selected from the group consisting of methyl, ethyl,    methoxymethyl, ethoxymethyl, prop-2-enyl, prop-2-ynyl,    methoxycarbonylmethyl and benzyl;-   R⁷ is selected from the group consisting of methyl, ethyl, propyl,    methoxymethyl, methoxyethyl and ethoxymethyl.

In another preferred embodiment of the present invention, X is CR² andthe variables R¹, R², R³, R⁴, R⁵, R⁶ and R⁷ have the following meanings:

-   R¹ is selected from the group consisting of chlorine, nitro, methyl,    cyclopropyl, trifluoromethyl, methoxymethyl, CH₂OCH₂CH₂OCH₃ and    methylsulfonyl;-   R² is selected from the group consisting of hydrogen, chlorine,    fluorine, methyl, CH₂OCH₂CF₃, methylsulfonyl, ethylsulfonyl,    methylsulfanyl, ethylsulfanyl, 3-isoxazolinyl,    5-methyl-3-isoxazolinyl, 5-isoxazolinyl, 3-methyl-5-isoxazolinyl,    3-isoxazolyl, 5-methyl-3-isoxazolyl, 5-isoxazolyl and    3-methyl-5-isoxazolyl;-   R³ is selected from the group consisting of hydrogen, fluorine,    chlorine, cyano, nitro, methyl, trifluoromethyl and methylsulfonyl;-   R⁴ is selected from the group consisting of hydrogen, cyano, methyl,    chlorine and fluorine;-   R⁵ is selected from the group consisting of chlorine and fluorine;-   R⁶ is selected from the group consisting of methyl, ethyl,    methoxymethyl, ethoxymethyl, prop-2-ynyl and methoxycarbonylmethyl;-   R⁷ is selected from the group consisting of methyl, ethyl and    methoxyethyl.

In a still further embodiment of the present invention, X is CR² and thevariable R³ is not hydrogen, in particular X is CR² and the variables R²and R³ are not hydrogen.

A second aspect of the present invention relates to a compositioncomprising at least one compound, an N-oxide or an agriculturallysuitable salt thereof, according to the present invention and at leastone auxiliary, which is customary for formulating crop protectioncompounds.

A further aspect of the present invention refers to the use of acompound, an N-oxide or an agriculturally suitable salt thereof, or acomposition according to the present invention for controlling unwantedvegetation.

A still further aspect of the present invention relates to a method forcontrolling unwanted vegetation which comprises allowing a herbicidallyeffective amount of at least one compound, an N-oxide or anagriculturally suitable salt thereof, or a composition according to thepresent invention to act on plants, their seed and/or their habitat.

According to another preferred embodiment of the invention, where X isCR², the variables R¹, R², R³, R⁴ and R⁵ together form one of thefollowing substitution patterns on the phenyl ring of compounds offormula I, provided that position 1 is the attachment point of thephenyl ring to the remainder of the molecule:

2-Br-4,6-Cl₂, 2,6-Cl₂-4-CN, 2,4,6-Cl₃, 2,6-Cl₂-4-F, 2,6-Cl₂-4-CF₃,2,6-Cl₂-4-S(O)₂CH₃, 2-CF₃-4-CN-6-Cl, 2-CF₃-4,6-Cl₂, 2-CF₃-4-CF₃-6-Cl,2-CF₃-4-S(O)₂CH₃-6-Cl, 2-CF₃-4-F-6-Cl, 2-CH₃—CN-6-Cl, 2-CH₃-4,6-Cl₂,2-CH₃-4-CF₃-6-Cl, 2-CH₃-4-S(O)₂CH₃-6-Cl, 2-CH₃-4-F-6-Cl,2-S(O)₂CH₃-4-CN-6-Cl, 2-S(O)₂CH₃-4,6-Cl₂, 2-S(O)₂CH₃-4-CF₃-6-Cl,2-S(O)₂CH₃-4-S(O)₂CH₃- 6-Cl, 2-S(O)₂CH₃-4-F-6-Cl, 2-Cl-4-CN-6-F,2-Cl-4-CF₃-6-F, 2-Cl-4-S(O)₂CH₃-6-F, 2,4-Cl₂-6-F, 2-Cl-4,6-F₂,2-CF₃-4-CN-6-F, 2-CF₃-4-CF₃-6-F, 2-CF₃-4-S(O)₂CH₃-6-F, 2-CF₃-4-Cl-6-F,2-CF₃-4,6-F₂, 2-CH₃-4-CN-6-F, 2-CH₃-4-CF₃-6-F, 2-CH₃-4-S(O)₂CH₃-6-F,2-CH₃-4-Cl-6-F, 2-CH₃-4,6- F₂, 2-S(O)₂CH₃-4-CN-6-F,2-S(O)₂CH₃-4-CF₃-6-F, 2-S(O)₂CH₃-4-S(O)₂CH₃-6-F, 2-S(O)₂CH₃-4- Cl-6-F or2-S(O)₂CH₃-4,6-F₂.

According to another preferred embodiment of the invention the variablesR¹, R², R³, R⁴ and R⁵ together form one of the following substitutionpatterns on the phenyl ring of compounds of formula I, provided thatposition 1 is the attachment point of the phenyl ring to the remainderof the molecule:

2,6-Cl₂-3-(3-isoxazolinyl)-4-CN, 2,4,6-Cl₃-3-(3-isoxazolinyl),2,6-Cl₂-3-(3-isoxazolinyl)-4-F, 2,6-Cl₂-3-(3-isoxazolinyl)-4-CF₃,2,6-Cl₂-3-(3-isoxazolinyl)-4-S(O)₂CH₃,2-CF₃-3-(3-isoxazolinyl)-4-CN-6-Cl, 2-CF₃-3-(3-isoxazolinyl)-4,6-Cl₂,2-CF₃-3-(3-isoxazolinyl)-4-CF₃-6-Cl,2-CF₃-3-(3-isoxazolinyl)-4-S(O)₂CH₃-6-Cl,2-CF₃-3-(3-isoxazolinyl)-4-F-6-Cl, 2-CH₃-3-(3-isoxazolinyl)-4-CN-6-Cl,2-CH₃-3-(3-isoxazolinyl)-4,6-Cl₂, 2-CH₃-3-(3-isoxazolinyl)-4-CF₃-6-Cl,2-CH₃-3-(3-isoxazolinyl)-4-S(O)₂CH₃-6-Cl,2-CH₃-3-(3-isoxazolinyl)-4-F-6-Cl,2-S(O)₂CH₃-3-(3-isoxazolinyl)-4-CN-6-Cl,2-S(O)₂CH₃-3-(3-isoxazolinyl)-4,6-Cl₂,2-S(O)₂CH₃-3-(3-isoxazolinyl)-4-CF₃-6-Cl,2-S(O)₂CH₃-3-(3-isoxazolinyl)-4-S(O)₂CH₃-6-Cl,2-S(O)₂CH₃-3-(3-isoxazolinyl)-4-F-6-Cl,2-Cl-3-(3-isoxazolinyl)-4-CN-6-F, 2-Cl-3-(3-isoxazolinyl)-4-CF₃-6-F,2-Cl-3-(3-isoxazolinyl)-4-S(O)₂CH₃-6-F, 2,4-Cl₂-3-(3-isoxazolinyl)-6-F,2-Cl-3-(3-isoxazolinyl)-4,6-F₂, 2-CF₃-3-(3-isoxazolinyl)-4-CN-6-F,2-CF₃-3-(3-isoxazolinyl)-4-CF₃-6-F,2-CF₃-3-(3-isoxazolinyl)-4-S(O)₂CH₃-6-F,2-CF₃-3-(3-isoxazolinyl)-4-Cl-6-F, 2-CF₃-3-(3-isoxazolinyl)-4,6-F₂,2-CH₃-3-(3-isoxazolinyl)-4-CN-6-F, 2-CH₃-3-(3-isoxazolinyl)-4-CF₃-6-F,2-CH₃-3-(3-isoxazolinyl)-4-S(O)₂CH₃-6-F,2-CH₃-3-(3-isoxazolinyl)-4-Cl-6-F, 2-CH₃-3-(3-isoxazolinyl)-4,6-F₂,2-S(O)₂CH₃-3-(3-isoxazolinyl)-4-CN-6-F,2-S(O)₂CH₃-3-(3-isoxazolinyl)-4-CF₃-6-F,2-S(O)₂CH₃-3-(3-isoxazolinyl)-4-S(O)₂CH₃-6-F,2-S(O)₂CH₃-3-(3-isoxazolinyl)-4-Cl-6-F,2-S(O)₂CH₃-3-(3-isoxazolinyl)-4,6-F₂, 2,6-Cl₂-3-(CH₂—O—CH₂CF₃)-4-CN,2,4,6-Cl₃-3-(3-isoxazolinyl), 2,6-Cl₂-3-(CH₂—O—CH₂CF₃)-4-F,2,6-Cl₂-3-(CH₂—O—CH₂CF₃)-4-CF₃, 2,6-Cl₂-3-(CH₂—O—CH₂CF₃)-4-S(O)₂CH₃,2-CF₃-3-(CH₂—O—CH₂CF₃)-4-CN-6-Cl, 2-CF₃-3-(CH₂—O—CH₂CF₃)-4,6-Cl₂,2-CF₃-3-(CH₂—O—CH₂CF₃)-4-CF₃-6-Cl,2-CF₃-3-(CH₂—O—CH₂CF₃)-4-S(O)₂CH₃-6-Cl, 2-CF₃-3-(CH₂—O—CH₂CF₃)-4-F-6-Cl,2-CH₃-3-(CH₂—O—CH₂CF₃)-4-CN-6-Cl, 2-CH₃-3-(CH₂—O—CH₂CF₃)-4,6-Cl₂,2-CH₃-3-(CH₂—O—CH₂CF₃)-4-CF₃-6-Cl,2-CH₃-3-(CH₂—O—CH₂CF₃)-4-S(O)₂CH₃-6-Cl, 2-CH₃-3-(CH₂—O—CH₂CF₃)-4-F-6-Cl,2-S(O)₂CH₃-3-(CH₂—O—CH₂CF₃)-4-CN-6-Cl,2-S(O)₂CH₃-3-(CH₂—O—CH₂CF₃)-4,6-Cl₂, 2-S(O)₂CH₃-3-(CH₂—O—CH₂CF₃)-4-CF₃-6-Cl, 2-S(O)₂CH₃-3-(CH₂—O—CH₂CF₃)-4-S(O)₂CH₃-6-Cl,2-S(O)₂CH₃-3-(CH₂—O—CH₂CF₃)-4-F-6-Cl, 2-Cl-3-(CH₂—O—CH₂CF₃)-4-CN-6-F,2-Cl-3-(CH₂—O—CH₂CF₃)-4-CF₃-6-F, 2-Cl-3-(CH₂—O—CH₂CF₃)- 4-S(O)₂CH₃-6-F,2,4-Cl₂-3-(CH₂—O—CH₂CF₃)-6-F, 2-Cl-3-(CH₂—O—CH₂CF₃)-4,6-F₂,2-CF₃-3-(CH₂—O—CH₂CF₃)-4-CN-6-F, 2-CF₃-3-(CH₂—O—CH₂CF₃)-4-CF₃-6-F,2-CF₃-3-(CH₂—O—CH₂CF₃)-4- S(O)₂CH₃-6-F, 2-CF₃-3-(CH₂—O—CH₂CF₃)-4-Cl-6-F,2-CF₃-3-(CH₂—O—CH₂CF₃)-4,6-F₂, 2-CH₃-3-(CH₂—O—CH₂CF₃)-4-CN-6-F,2-CH₃-3-(CH₂—O—CH₂CF₃)-4-CF₃-6-F, 2-CH₃-3-(CH₂—O—CH₂CF₃)-4-S(O)₂CH₃-6-F,2-CH₃-3-(CH₂—O—CH₂CF₃)-4-Cl-6-F, 2-CH₃-3-(CH₂—O—CH₂CF₃)-4,6-F₂,2-S(O)₂CH₃-3-(CH₂—O—CH₂CF₃)-4-CN-6-F,2-S(O)₂CH₃-3-(CH₂—O—CH₂CF₃)-4-CF₃-6-F, 2-S(O)₂CH₃-3-(CH₂—O—CH₂CF₃)-4-S(O)₂CH₃-6-F,2-S(O)₂CH₃-3-(CH₂—O—CH₂CF₃)-4-Cl-6-F or2-S(O)₂CH₃-3-(CH₂—O—CH₂CF₃)-4,6-F₂.

Examples of preferred compounds I.A, where X is N, are the individualcompounds compiled in Tables 1 to 20 below. Moreover, the meaningsmentioned below for the individual variables in the Tables are per se,independently of the combination in which they are mentioned, aparticularly preferred embodiment of the substituents in question.

Table 1 Compounds of formula I.A (I.A-1.1-I.A-1.2304) in which B is CH,R⁴ is H and R⁵ is F and the combination of R¹, R³, R⁶ and R⁷ for acompound corresponds in each case to one row of Table A;Table 2 Compounds of formula I.A (I.A-2.1-I.A-2.2304) in which B is CH,R⁴ is H and R⁵ is Cl and the combination of R¹, R³, R⁶ and R⁷ for acompound corresponds in each case to one row of Table A;Table 3 Compounds of formula I.A (I.A-3.1-I.A-3.2304) in which B is CH,R⁴ is F and R⁵ is F and the combination of R¹, R³, R⁶ and R⁷ for acompound corresponds in each case to one row of Table A;Table 4 Compounds of formula I.A (I.A-4.1-I.A-4.2304) in which B is CH,R⁴ is F and R⁵ is Cl and the combination of R¹, R³, R⁶ and R⁷ for acompound corresponds in each case to one row of Table A;Table 5 Compounds of formula I.A (I.A-5.1-I.A-5.2304) in which B is CH,R⁴ is Cl and R⁵ is F and the combination of R¹, R³, R⁶ and R⁷ for acompound corresponds in each case to one row of Table A;Table 6 Compounds of formula I.A (I.A-6.1-I.A-6.2304) in which B is CH,R⁴ is Cl and R⁵ is Cl and the combination of R¹, R³, R⁶ and R⁷ for acompound corresponds in each case to one row of Table A;Table 7 Compounds of formula I.A (I.A-7.1-I.A-7.2304) in which B is CH,R⁴ is CN and R⁵ is F and the combination of R¹, R³, R⁶ and R⁷ for acompound corresponds in each case to one row of Table A;Table 8 Compounds of formula I.A (I.A-8.1-I.A-8.2304) in which B is CH,R⁴ is CN and R⁵ is Cl and the combination of R¹, R³, R⁶ and R⁷ for acompound corresponds in each case to one row of Table A;Table 9 Compounds of formula I.A (I.A-9.1-I.A-9.2304) in which B is CH,R⁴ is CH₃ and R⁵ is F and the combination of R¹, R³, R⁶ and R⁷ for acompound corresponds in each case to one row of Table A;Table 10 Compounds of formula I.A (I.A-10.1-I.A-10.2304) in which B isCH, R⁴ is CH₃ and R⁵ is Cl and the combination of R¹, R³, R⁶ and R⁷ fora compound corresponds in each case to one row of Table A;Table 11 Compounds of formula I.A (I.A-11.1-I.A-11.2304) in which B isN, R⁴ is H and R⁵ is F and the combination of R¹, R³, R⁶ and R⁷ for acompound corresponds in each case to one row of Table A;Table 12 Compounds of formula I.A (I.A-12.1-I.A-12.2304) in which B isN, R⁴ is H and R⁵ is Cl and the combination of R¹, R³, R⁶ and R⁷ for acompound corresponds in each case to one row of Table A;Table 13 Compounds of formula I.A (I.A-13.1-I.A-13.2304) in which B isN, R⁴ is F and R⁵ is F and the combination of R¹, R³, R⁶ and R⁷ for acompound corresponds in each case to one row of Table A;Table 14 Compounds of formula I.A (I.A-14.1-I.A-14.2304) in which B isN, R⁴ is F and R⁵ is Cl and the combination of R¹, R³, R⁶ and R⁷ for acompound corresponds in each case to one row of Table A;Table 15 Compounds of formula I.A (I.A-15.1-I.A-15.2304) in which B isN, R⁴ is Cl and R⁵ is F and the combination of R¹, R³, R⁶ and R⁷ for acompound corresponds in each case to one row of Table A;Table 16 Compounds of formula I.A (I.A-16.1-I.A-16.2304) in which B isN, R⁴ is Cl and R⁵ is Cl and the combination of R¹, R³, R⁶ and R⁷ for acompound corresponds in each case to one row of Table A;Table 17 Compounds of formula I.A (I.A-17.1-I.A-17.2304) in which B isN, R⁴ is CN and R⁵ is F and the combination of R¹, R³, R⁶ and R⁷ for acompound corresponds in each case to one row of Table A;Table 18 Compounds of formula I.A (I.A-18.1-I.A-18.2304) in which B isN, R⁴ is CN and R⁵ is Cl and the combination of R¹, R³, R⁶ and R⁷ for acompound corresponds in each case to one row of Table A;Table 19 Compounds of formula I.A (I.A-19.1-I.A-19.2304) in which B isN, R⁴ is CH₃ and R⁵ is F and the combination of R¹, R³, R⁶ and R⁷ for acompound corresponds in each case to one row of Table A;Table 20 Compounds of formula I.A (I.A-20.1-I.A-20.2304) in which B isN, R⁴ is CH₃ and R⁵ is Cl and the combination of R¹, R³, R⁶ and R⁷ for acompound corresponds in each case to one row of Table A;

TABLE A R¹ R³ R⁶ R⁷ A-1 Cl H CH₃ CH₃ A-2 Cl H CH₃ CH₂CH₃ A-3 Cl H CH₃CH₂CH₂CH₃ A-4 Cl H CH₃ CH₂CH₂OCH₃ A-5 Cl H CH₂CH₃ CH₃ A-6 Cl H CH₂CH₃CH₂CH₃ A-7 Cl H CH₂CH₃ CH₂CH₂CH₃ A-8 Cl H CH₂CH₃ CH₂CH₂OCH₃ A-9 Cl HCH₂OCH₃ CH₃ A-10 Cl H CH₂OCH₃ CH₂CH₃ A-11 Cl H CH₂OCH₃ CH₂CH₂CH₃ A-12 ClH CH₂OCH₃ CH₂CH₂OCH₃ A-13 Cl H CH₂OCH₂CH₃ CH₃ A-14 Cl H CH₂OCH₂CH₃CH₂CH₃ A-15 Cl H CH₂OCH₂CH₃ CH₂CH₂CH₃ A-16 Cl H CH₂OCH₂CH₃ CH₂CH₂OCH₃A-17 Cl H CH₂(CO)OCH₃ CH₃ A-18 Cl H CH₂(CO)OCH₃ CH₂CH₃ A-19 Cl HCH₂(CO)OCH₃ CH₂CH₂CH₃ A-20 Cl H CH₂(CO)OCH₃ CH₂CH₂OCH₃ A-21 Cl HCH₂CHCH₂ CH₃ A-22 Cl H CH₂CHCH₂ CH₂CH₃ A-23 Cl H CH₂CHCH₂ CH₂CH₂CH₃ A-24Cl H CH₂CHCH₂ CH₂CH₂OCH₃ A-25 Cl H CH₂CCH CH₃ A-26 Cl H CH₂CCH CH₂CH₃A-27 Cl H CH₂CCH CH₂CH₂CH₃ A-28 Cl H CH₂CCH CH₂CH₂OCH₃ A-29 Cl H CH₂C₆H₅CH₃ A-30 Cl H CH₂C₆H₅ CH₂CH₃ A-31 Cl H CH₂C₆H₅ CH₂CH₂CH₃ A-32 Cl HCH₂C₆H₅ CH₂CH₂OCH₃ A-33 Cl F CH₃ CH₃ A-34 Cl F CH₃ CH₂CH₃ A-35 Cl F CH₃CH₂CH₂CH₃ A-36 Cl F CH₃ CH₂CH₂OCH₃ A-37 Cl F CH₂CH₃ CH₃ A-38 Cl F CH₂CH₃CH₂CH₃ A-39 Cl F CH₂CH₃ CH₂CH₂CH₃ A-40 Cl F CH₂CH₃ CH₂CH₂OCH₃ A-41 Cl FCH₂OCH₃ CH₃ A-42 Cl F CH₂OCH₃ CH₂CH₃ A-43 Cl F CH₂OCH₃ CH₂CH₂CH₃ A-44 ClF CH₂OCH₃ CH₂CH₂OCH₃ A-45 Cl F CH₂OCH₂CH₃ CH₃ A-46 Cl F CH₂OCH₂CH₃CH₂CH₃ A-47 Cl F CH₂OCH₂CH₃ CH₂CH₂CH₃ A-48 Cl F CH₂OCH₂CH₃ CH₂CH₂OCH₃A-49 Cl F CH₂(CO)OCH₃ CH₃ A-50 Cl F CH₂(CO)OCH₃ CH₂CH₃ A-51 Cl FCH₂(CO)OCH₃ CH₂CH₂CH₃ A-52 Cl F CH₂(CO)OCH₃ CH₂CH₂OCH₃ A-53 Cl FCH₂CHCH₂ CH₃ A-54 Cl F CH₂CHCH₂ CH₂CH₃ A-55 Cl F CH₂CHCH₂ CH₂CH₂CH₃ A-56Cl F CH₂CHCH₂ CH₂CH₂OCH₃ A-57 Cl F CH₂CCH CH₃ A-58 Cl F CH₂CCH CH₂CH₃A-59 Cl F CH₂CCH CH₂CH₂CH₃ A-60 Cl F CH₂CCH CH₂CH₂OCH₃ A-61 Cl F CH₂C₆H₅CH₃ A-62 Cl F CH₂C₆H₅ CH₂CH₃ A-63 Cl F CH₂C₆H₅ CH₂CH₂CH₃ A-64 Cl FCH₂C₆H₅ CH₂CH₂OCH₃ A-65 Cl Cl CH₃ CH₃ A-66 Cl Cl CH₃ CH₂CH₃ A-67 Cl ClCH₃ CH₂CH₂CH₃ A-68 Cl Cl CH₃ CH₂CH₂OCH₃ A-69 Cl Cl CH₂CH₃ CH₃ A-70 Cl ClCH₂CH₃ CH₂CH₃ A-71 Cl Cl CH₂CH₃ CH₂CH₂CH₃ A-72 Cl Cl CH₂CH₃ CH₂CH₂OCH₃A-73 Cl Cl CH₂OCH₃ CH₃ A-74 Cl Cl CH₂OCH₃ CH₂CH₃ A-75 Cl Cl CH₂OCH₃CH₂CH₂CH₃ A-76 Cl Cl CH₂OCH₃ CH₂CH₂OCH₃ A-77 Cl Cl CH₂OCH₂CH₃ CH₃ A-78Cl Cl CH₂OCH₂CH₃ CH₂CH₃ A-79 Cl Cl CH₂OCH₂CH₃ CH₂CH₂CH₃ A-80 Cl ClCH₂OCH₂CH₃ CH₂CH₂OCH₃ A-81 Cl Cl CH₂(CO)OCH₃ CH₃ A-82 Cl Cl CH₂(CO)OCH₃CH₂CH₃ A-83 Cl Cl CH₂(CO)OCH₃ CH₂CH₂CH₃ A-84 Cl Cl CH₂(CO)OCH₃CH₂CH₂OCH₃ A-85 Cl Cl CH₂CHCH₂ CH₃ A-86 Cl Cl CH₂CHCH₂ CH₂CH₃ A-87 Cl ClCH₂CHCH₂ CH₂CH₂CH₃ A-88 Cl Cl CH₂CHCH₂ CH₂CH₂OCH₃ A-89 Cl Cl CH₂CCH CH₃A-90 Cl Cl CH₂CCH CH₂CH₃ A-91 Cl Cl CH₂CCH CH₂CH₂CH₃ A-92 Cl Cl CH₂CCHCH₂CH₂OCH₃ A-93 Cl Cl CH₂C₆H₅ CH₃ A-94 Cl Cl CH₂C₆H₅ CH₂CH₃ A-95 Cl ClCH₂C₆H₅ CH₂CH₂CH₃ A-96 Cl Cl CH₂C₆H₅ CH₂CH₂OCH₃ A-97 Cl Br CH₃ CH₃ A-98Cl Br CH₃ CH₂CH₃ A-99 Cl Br CH₃ CH₂CH₂CH₃ A-100 Cl Br CH₃ CH₂CH₂OCH₃A-101 Cl Br CH₂CH₃ CH₃ A-102 Cl Br CH₂CH₃ CH₂CH₃ A-103 Cl Br CH₂CH₃CH₂CH₂CH₃ A-104 Cl Br CH₂CH₃ CH₂CH₂OCH₃ A-105 Cl Br CH₂OCH₃ CH₃ A-106 ClBr CH₂OCH₃ CH₂CH₃ A-107 Cl Br CH₂OCH₃ CH₂CH₂CH₃ A-108 Cl Br CH₂OCH₃CH₂CH₂OCH₃ A-109 Cl Br CH₂OCH₂CH₃ CH₃ A-110 Cl Br CH₂OCH₂CH₃ CH₂CH₃A-111 Cl Br CH₂OCH₂CH₃ CH₂CH₂CH₃ A-112 Cl Br CH₂OCH₂CH₃ CH₂CH₂OCH₃ A-113Cl Br CH₂(CO)OCH₃ CH₃ A-114 Cl Br CH₂(CO)OCH₃ CH₂CH₃ A-115 Cl BrCH₂(CO)OCH₃ CH₂CH₂CH₃ A-116 Cl Br CH₂(CO)OCH₃ CH₂CH₂OCH₃ A-117 Cl BrCH₂CHCH₂ CH₃ A-118 Cl Br CH₂CHCH₂ CH₂CH₃ A-119 Cl Br CH₂CHCH₂ CH₂CH₂CH₃A-120 Cl Br CH₂CHCH₂ CH₂CH₂OCH₃ A-121 Cl Br CH₂CCH CH₃ A-122 Cl BrCH₂CCH CH₂CH₃ A-123 Cl Br CH₂CCH CH₂CH₂CH₃ A-124 Cl Br CH₂CCH CH₂CH₂OCH₃A-125 Cl Br CH₂C₆H₅ CH₃ A-126 Cl Br CH₂C₆H₅ CH₂CH₃ A-127 Cl Br CH₂C₆H₅CH₂CH₂CH₃ A-128 Cl Br CH₂C₆H₅ CH₂CH₂OCH₃ A-129 Cl CN CH₃ CH₃ A-130 Cl CNCH₃ CH₂CH₃ A-131 Cl CN CH₃ CH₂CH₂CH₃ A-132 Cl CN CH₃ CH₂CH₂OCH₃ A-133 ClCN CH₂CH₃ CH₃ A-134 Cl CN CH₂CH₃ CH₂CH₃ A-135 Cl CN CH₂CH₃ CH₂CH₂CH₃A-136 Cl CN CH₂CH₃ CH₂CH₂OCH₃ A-137 Cl CN CH₂OCH₃ CH₃ A-138 Cl CNCH₂OCH₃ CH₂CH₃ A-139 Cl CN CH₂OCH₃ CH₂CH₂CH₃ A-140 Cl CN CH₂OCH₃CH₂CH₂OCH₃ A-141 Cl CN CH₂OCH₂CH₃ CH₃ A-142 Cl CN CH₂OCH₂CH₃ CH₂CH₃A-143 Cl CN CH₂OCH₂CH₃ CH₂CH₂CH₃ A-144 Cl CN CH₂OCH₂CH₃ CH₂CH₂OCH₃ A-145Cl CN CH₂(CO)OCH₃ CH₃ A-146 Cl CN CH₂(CO)OCH₃ CH₂CH₃ A-147 Cl CNCH₂(CO)OCH₃ CH₂CH₂CH₃ A-148 Cl CN CH₂(CO)OCH₃ CH₂CH₂OCH₃ A-149 Cl CNCH₂CHCH₂ CH₃ A-150 Cl CN CH₂CHCH₂ CH₂CH₃ A-151 Cl CN CH₂CHCH₂ CH₂CH₂CH₃A-152 Cl CN CH₂CHCH₂ CH₂CH₂OCH₃ A-153 Cl CN CH₂CCH CH₃ A-154 Cl CNCH₂CCH CH₂CH₃ A-155 Cl CN CH₂CCH CH₂CH₂CH₃ A-156 Cl CN CH₂CCH CH₂CH₂OCH₃A-157 Cl CN CH₂C₆H₅ CH₃ A-158 Cl CN CH₂C₆H₅ CH₂CH₃ A-159 Cl CN CH₂C₆H₅CH₂CH₂CH₃ A-160 Cl CN CH₂C₆H₅ CH₂CH₂OCH₃ A-161 Cl CH₃ CH₃ CH₃ A-162 ClCH₃ CH₃ CH₂CH₃ A-163 Cl CH₃ CH₃ CH₂CH₂CH₃ A-164 Cl CH₃ CH₃ CH₂CH₂OCH₃A-165 Cl CH₃ CH₂CH₃ CH₃ A-166 Cl CH₃ CH₂CH₃ CH₂CH₃ A-167 Cl CH₃ CH₂CH₃CH₂CH₂CH₃ A-168 Cl CH₃ CH₂CH₃ CH₂CH₂OCH₃ A-169 Cl CH₃ CH₂OCH₃ CH₃ A-170Cl CH₃ CH₂OCH₃ CH₂CH₃ A-171 Cl CH₃ CH₂OCH₃ CH₂CH₂CH₃ A-172 Cl CH₃CH₂OCH₃ CH₂CH₂OCH₃ A-173 Cl CH₃ CH₂OCH₂CH₃ CH₃ A-174 Cl CH₃ CH₂OCH₂CH₃CH₂CH₃ A-175 Cl CH₃ CH₂OCH₂CH₃ CH₂CH₂CH₃ A-176 Cl CH₃ CH₂OCH₂CH₃CH₂CH₂OCH₃ A-177 Cl CH₃ CH₂(CO)OCH₃ CH₃ A-178 Cl CH₃ CH₂(CO)OCH₃ CH₂CH₃A-179 Cl CH₃ CH₂(CO)OCH₃ CH₂CH₂CH₃ A-180 Cl CH₃ CH₂(CO)OCH₃ CH₂CH₂OCH₃A-181 Cl CH₃ CH₂CHCH₂ CH₃ A-182 Cl CH₃ CH₂CHCH₂ CH₂CH₃ A-183 Cl CH₃CH₂CHCH₂ CH₂CH₂CH₃ A-184 Cl CH₃ CH₂CHCH₂ CH₂CH₂OCH₃ A-185 Cl CH₃ CH₂CCHCH₃ A-186 Cl CH₃ CH₂CCH CH₂CH₃ A-187 Cl CH₃ CH₂CCH CH₂CH₂CH₃ A-188 ClCH₃ CH₂CCH CH₂CH₂OCH₃ A-189 Cl CH₃ CH₂C₆H₅ CH₃ A-190 Cl CH₃ CH₂C₆H₅CH₂CH₃ A-191 Cl CH₃ CH₂C₆H₅ CH₂CH₂CH₃ A-192 Cl CH₃ CH₂C₆H₅ CH₂CH₂OCH₃A-193 Cl CF₃ CH₃ CH₃ A-194 Cl CF₃ CH₃ CH₂CH₃ A-195 Cl CF₃ CH₃ CH₂CH₂CH₃A-196 Cl CF₃ CH₃ CH₂CH₂OCH₃ A-197 Cl CF₃ CH₂CH₃ CH₃ A-198 Cl CF₃ CH₂CH₃CH₂CH₃ A-199 Cl CF₃ CH₂CH₃ CH₂CH₂CH₃ A-200 Cl CF₃ CH₂CH₃ CH₂CH₂OCH₃A-201 Cl CF₃ CH₂OCH₃ CH₃ A-202 Cl CF₃ CH₂OCH₃ CH₂CH₃ A-203 Cl CF₃CH₂OCH₃ CH₂CH₂CH₃ A-204 Cl CF₃ CH₂OCH₃ CH₂CH₂OCH₃ A-205 Cl CF₃CH₂OCH₂CH₃ CH₃ A-206 Cl CF₃ CH₂OCH₂CH₃ CH₂CH₃ A-207 Cl CF₃ CH₂OCH₂CH₃CH₂CH₂CH₃ A-208 Cl CF₃ CH₂OCH₂CH₃ CH₂CH₂OCH₃ A-209 Cl CF₃ CH₂(CO)OCH₃CH₃ A-210 Cl CF₃ CH₂(CO)OCH₃ CH₂CH₃ A-211 Cl CF₃ CH₂(CO)OCH₃ CH₂CH₂CH₃A-212 Cl CF₃ CH₂(CO)OCH₃ CH₂CH₂OCH₃ A-213 Cl CF₃ CH₂CHCH₂ CH₃ A-214 ClCF₃ CH₂CHCH₂ CH₂CH₃ A-215 Cl CF₃ CH₂CHCH₂ CH₂CH₂CH₃ A-216 Cl CF₃CH₂CHCH₂ CH₂CH₂OCH₃ A-217 Cl CF₃ CH₂CCH CH₃ A-218 Cl CF₃ CH₂CCH CH₂CH₃A-219 Cl CF₃ CH₂CCH CH₂CH₂CH₃ A-220 Cl CF₃ CH₂CCH CH₂CH₂OCH₃ A-221 ClCF₃ CH₂C₆H₅ CH₃ A-222 Cl CF₃ CH₂C₆H₅ CH₂CH₃ A-223 Cl CF₃ CH₂C₆H₅CH₂CH₂CH₃ A-224 Cl CF₃ CH₂C₆H₅ CH₂CH₂OCH₃ A-225 Cl SO₂CH₃ CH₃ CH₃ A-226Cl SO₂CH₃ CH₃ CH₂CH₃ A-227 Cl SO₂CH₃ CH₃ CH₂CH₂CH₃ A-228 Cl SO₂CH₃ CH₃CH₂CH₂OCH₃ A-229 Cl SO₂CH₃ CH₂CH₃ CH₃ A-230 Cl SO₂CH₃ CH₂CH₃ CH₂CH₃A-231 Cl SO₂CH₃ CH₂CH₃ CH₂CH₂CH₃ A-232 Cl SO₂CH₃ CH₂CH₃ CH₂CH₂OCH₃ A-233Cl SO₂CH₃ CH₂OCH₃ CH₃ A-234 Cl SO₂CH₃ CH₂OCH₃ CH₂CH₃ A-235 Cl SO₂CH₃CH₂OCH₃ CH₂CH₂CH₃ A-236 Cl SO₂CH₃ CH₂OCH₃ CH₂CH₂OCH₃ A-237 Cl SO₂CH₃CH₂OCH₂CH₃ CH₃ A-238 Cl SO₂CH₃ CH₂OCH₂CH₃ CH₂CH₃ A-239 Cl SO₂CH₃CH₂OCH₂CH₃ CH₂CH₂CH₃ A-240 Cl SO₂CH₃ CH₂OCH₂CH₃ CH₂CH₂OCH₃ A-241 ClSO₂CH₃ CH₂(CO)OCH₃ CH₃ A-242 Cl SO₂CH₃ CH₂(CO)OCH₃ CH₂CH₃ A-243 ClSO₂CH₃ CH₂(CO)OCH₃ CH₂CH₂CH₃ A-244 Cl SO₂CH₃ CH₂(CO)OCH₃ CH₂CH₂OCH₃A-245 Cl SO₂CH₃ CH₂CHCH₂ CH₃ A-246 Cl SO₂CH₃ CH₂CHCH₂ CH₂CH₃ A-247 ClSO₂CH₃ CH₂CHCH₂ CH₂CH₂CH₃ A-248 Cl SO₂CH₃ CH₂CHCH₂ CH₂CH₂OCH₃ A-249 ClSO₂CH₃ CH₂CCH CH₃ A-250 Cl SO₂CH₃ CH₂CCH CH₂CH₃ A-251 Cl SO₂CH₃ CH₂CCHCH₂CH₂CH₃ A-252 Cl SO₂CH₃ CH₂CCH CH₂CH₂OCH₃ A-253 Cl SO₂CH₃ CH₂C₆H₅ CH₃A-254 Cl SO₂CH₃ CH₂C₆H₅ CH₂CH₃ A-255 Cl SO₂CH₃ CH₂C₆H₅ CH₂CH₂CH₃ A-256Cl SO₂CH₃ CH₂C₆H₅ CH₂CH₂OCH₃ A-257 Cl NO₂ CH₃ CH₃ A-258 Cl NO₂ CH₃CH₂CH₃ A-259 Cl NO₂ CH₃ CH₂CH₂CH₃ A-260 Cl NO₂ CH₃ CH₂CH₂OCH₃ A-261 ClNO₂ CH₂CH₃ CH₃ A-262 Cl NO₂ CH₂CH₃ CH₂CH₃ A-263 Cl NO₂ CH₂CH₃ CH₂CH₂CH₃A-264 Cl NO₂ CH₂CH₃ CH₂CH₂OCH₃ A-265 Cl NO₂ CH₂OCH₃ CH₃ A-266 Cl NO₂CH₂OCH₃ CH₂CH₃ A-267 Cl NO₂ CH₂OCH₃ CH₂CH₂CH₃ A-268 Cl NO₂ CH₂OCH₃CH₂CH₂OCH₃ A-269 Cl NO₂ CH₂OCH₂CH₃ CH₃ A-270 Cl NO₂ CH₂OCH₂CH₃ CH₂CH₃A-271 Cl NO₂ CH₂OCH₂CH₃ CH₂CH₂CH₃ A-272 Cl NO₂ CH₂OCH₂CH₃ CH₂CH₂OCH₃A-273 Cl NO₂ CH₂(CO)OCH₃ CH₃ A-274 Cl NO₂ CH₂(CO)OCH₃ CH₂CH₃ A-275 ClNO₂ CH₂(CO)OCH₃ CH₂CH₂CH₃ A-276 Cl NO₂ CH₂(CO)OCH₃ CH₂CH₂OCH₃ A-277 ClNO₂ CH₂CHCH₂ CH₃ A-278 Cl NO₂ CH₂CHCH₂ CH₂CH₃ A-279 Cl NO₂ CH₂CHCH₂CH₂CH₂CH₃ A-280 Cl NO₂ CH₂CHCH₂ CH₂CH₂OCH₃ A-281 Cl NO₂ CH₂CCH CH₃ A-282Cl NO₂ CH₂CCH CH₂CH₃ A-283 Cl NO₂ CH₂CCH CH₂CH₂CH₃ A-284 Cl NO₂ CH₂CCHCH₂CH₂OCH₃ A-285 Cl NO₂ CH₂C₆H₅ CH₃ A-286 Cl NO₂ CH₂C₆H₅ CH₂CH₃ A-287 ClNO₂ CH₂C₆H₅ CH₂CH₂CH₃ A-288 Cl NO₂ CH₂C₆H₅ CH₂CH₂OCH₃ A-289 NO₂ H CH₃CH₃ A-290 NO₂ H CH₃ CH₂CH₃ A-291 NO₂ H CH₃ CH₂CH₂CH₃ A-292 NO₂ H CH₃CH₂CH₂OCH₃ A-293 NO₂ H CH₂CH₃ CH₃ A-294 NO₂ H CH₂CH₃ CH₂CH₃ A-295 NO₂ HCH₂CH₃ CH₂CH₂CH₃ A-296 NO₂ H CH₂CH₃ CH₂CH₂OCH₃ A-297 NO₂ H CH₂OCH₃ CH₃A-298 NO₂ H CH₂OCH₃ CH₂CH₃ A-299 NO₂ H CH₂OCH₃ CH₂CH₂CH₃ A-300 NO₂ HCH₂OCH₃ CH₂CH₂OCH₃ A-301 NO₂ H CH₂OCH₂CH₃ CH₃ A-302 NO₂ H CH₂OCH₂CH₃CH₂CH₃ A-303 NO₂ H CH₂OCH₂CH₃ CH₂CH₂CH₃ A-304 NO₂ H CH₂OCH₂CH₃CH₂CH₂OCH₃ A-305 NO₂ H CH₂(CO)OCH₃ CH₃ A-306 NO₂ H CH₂(CO)OCH₃ CH₂CH₃A-307 NO₂ H CH₂(CO)OCH₃ CH₂CH₂CH₃ A-308 NO₂ H CH₂(CO)OCH₃ CH₂CH₂OCH₃A-309 NO₂ H CH₂CHCH₂ CH₃ A-310 NO₂ H CH₂CHCH₂ CH₂CH₃ A-311 NO₂ HCH₂CHCH₂ CH₂CH₂CH₃ A-312 NO₂ H CH₂CHCH₂ CH₂CH₂OCH₃ A-313 NO₂ H CH₂CCHCH₃ A-314 NO₂ H CH₂CCH CH₂CH₃ A-315 NO₂ H CH₂CCH CH₂CH₂CH₃ A-316 NO₂ HCH₂CCH CH₂CH₂OCH₃ A-317 NO₂ H CH₂C₆H₅ CH₃ A-318 NO₂ H CH₂C₆H₅ CH₂CH₃A-319 NO₂ H CH₂C₆H₅ CH₂CH₂CH₃ A-320 NO₂ H CH₂C₆H₅ CH₂CH₂OCH₃ A-321 NO₂ FCH₃ CH₃ A-322 NO₂ F CH₃ CH₂CH₃ A-323 NO₂ F CH₃ CH₂CH₂CH₃ A-324 NO₂ F CH₃CH₂CH₂OCH₃ A-325 NO₂ F CH₂CH₃ CH₃ A-326 NO₂ F CH₂CH₃ CH₂CH₃ A-327 NO₂ FCH₂CH₃ CH₂CH₂CH₃ A-328 NO₂ F CH₂CH₃ CH₂CH₂OCH₃ A-329 NO₂ F CH₂OCH₃ CH₃A-330 NO₂ F CH₂OCH₃ CH₂CH₃ A-331 NO₂ F CH₂OCH₃ CH₂CH₂CH₃ A-332 NO₂ FCH₂OCH₃ CH₂CH₂OCH₃ A-333 NO₂ F CH₂OCH₂CH₃ CH₃ A-334 NO₂ F CH₂OCH₂CH₃CH₂CH₃ A-335 NO₂ F CH₂OCH₂CH₃ CH₂CH₂CH₃ A-336 NO₂ F CH₂OCH₂CH₃CH₂CH₂OCH₃ A-337 NO₂ F CH₂(CO)OCH₃ CH₃ A-338 NO₂ F CH₂(CO)OCH₃ CH₂CH₃A-339 NO₂ F CH₂(CO)OCH₃ CH₂CH₂CH₃ A-340 NO₂ F CH₂(CO)OCH₃ CH₂CH₂OCH₃A-341 NO₂ F CH₂CHCH₂ CH₃ A-342 NO₂ F CH₂CHCH₂ CH₂CH₃ A-343 NO₂ FCH₂CHCH₂ CH₂CH₂CH₃ A-344 NO₂ F CH₂CHCH₂ CH₂CH₂OCH₃ A-345 NO₂ F CH₂CCHCH₃ A-346 NO₂ F CH₂CCH CH₂CH₃ A-347 NO₂ F CH₂CCH CH₂CH₂CH₃ A-348 NO₂ FCH₂CCH CH₂CH₂OCH₃ A-349 NO₂ F CH₂C₆H₅ CH₃ A-350 NO₂ F CH₂C₆H₅ CH₂CH₃A-351 NO₂ F CH₂C₆H₅ CH₂CH₂CH₃ A-352 NO₂ F CH₂C₆H₅ CH₂CH₂OCH₃ A-353 NO₂Cl CH₃ CH₃ A-354 NO₂ Cl CH₃ CH₂CH₃ A-355 NO₂ Cl CH₃ CH₂CH₂CH₃ A-356 NO₂Cl CH₃ CH₂CH₂OCH₃ A-357 NO₂ Cl CH₂CH₃ CH₃ A-358 NO₂ Cl CH₂CH₃ CH₂CH₃A-359 NO₂ Cl CH₂CH₃ CH₂CH₂CH₃ A-360 NO₂ Cl CH₂CH₃ CH₂CH₂OCH₃ A-361 NO₂Cl CH₂OCH₃ CH₃ A-362 NO₂ Cl CH₂OCH₃ CH₂CH₃ A-363 NO₂ Cl CH₂OCH₃CH₂CH₂CH₃ A-364 NO₂ Cl CH₂OCH₃ CH₂CH₂OCH₃ A-365 NO₂ Cl CH₂OCH₂CH₃ CH₃A-366 NO₂ Cl CH₂OCH₂CH₃ CH₂CH₃ A-367 NO₂ Cl CH₂OCH₂CH₃ CH₂CH₂CH₃ A-368NO₂ Cl CH₂OCH₂CH₃ CH₂CH₂OCH₃ A-369 NO₂ Cl CH₂(CO)OCH₃ CH₃ A-370 NO₂ ClCH₂(CO)OCH₃ CH₂CH₃ A-371 NO₂ Cl CH₂(CO)OCH₃ CH₂CH₂CH₃ A-372 NO₂ ClCH₂(CO)OCH₃ CH₂CH₂OCH₃ A-373 NO₂ Cl CH₂CHCH₂ CH₃ A-374 NO₂ Cl CH₂CHCH₂CH₂CH₃ A-375 NO₂ Cl CH₂CHCH₂ CH₂CH₂CH₃ A-376 NO₂ Cl CH₂CHCH₂ CH₂CH₂OCH₃A-377 NO₂ Cl CH₂CCH CH₃ A-378 NO₂ Cl CH₂CCH CH₂CH₃ A-379 NO₂ Cl CH₂CCHCH₂CH₂CH₃ A-380 NO₂ Cl CH₂CCH CH₂CH₂OCH₃ A-381 NO₂ Cl CH₂C₆H₅ CH₃ A-382NO₂ Cl CH₂C₆H₅ CH₂CH₃ A-383 NO₂ Cl CH₂C₆H₅ CH₂CH₂CH₃ A-384 NO₂ ClCH₂C₆H₅ CH₂CH₂OCH₃ A-385 NO₂ Br CH₃ CH₃ A-386 NO₂ Br CH₃ CH₂CH₃ A-387NO₂ Br CH₃ CH₂CH₂CH₃ A-388 NO₂ Br CH₃ CH₂CH₂OCH₃ A-389 NO₂ Br CH₂CH₃ CH₃A-390 NO₂ Br CH₂CH₃ CH₂CH₃ A-391 NO₂ Br CH₂CH₃ CH₂CH₂CH₃ A-392 NO₂ BrCH₂CH₃ CH₂CH₂OCH₃ A-393 NO₂ Br CH₂OCH₃ CH₃ A-394 NO₂ Br CH₂OCH₃ CH₂CH₃A-395 NO₂ Br CH₂OCH₃ CH₂CH₂CH₃ A-396 NO₂ Br CH₂OCH₃ CH₂CH₂OCH₃ A-397 NO₂Br CH₂OCH₂CH₃ CH₃ A-398 NO₂ Br CH₂OCH₂CH₃ CH₂CH₃ A-399 NO₂ Br CH₂OCH₂CH₃CH₂CH₂CH₃ A-400 NO₂ Br CH₂OCH₂CH₃ CH₂CH₂OCH₃ A-401 NO₂ Br CH₂(CO)OCH₃CH₃ A-402 NO₂ Br CH₂(CO)OCH₃ CH₂CH₃ A-403 NO₂ Br CH₂(CO)OCH₃ CH₂CH₂CH₃A-404 NO₂ Br CH₂(CO)OCH₃ CH₂CH₂OCH₃ A-405 NO₂ Br CH₂CHCH₂ CH₃ A-406 NO₂Br CH₂CHCH₂ CH₂CH₃ A-407 NO₂ Br CH₂CHCH₂ CH₂CH₂CH₃ A-408 NO₂ Br CH₂CHCH₂CH₂CH₂OCH₃ A-409 NO₂ Br CH₂CCH CH₃ A-410 NO₂ Br CH₂CCH CH₂CH₃ A-411 NO₂Br CH₂CCH CH₂CH₂CH₃ A-412 NO₂ Br CH₂CCH CH₂CH₂OCH₃ A-413 NO₂ Br CH₂C₆H₅CH₃ A-414 NO₂ Br CH₂C₆H₅ CH₂CH₃ A-415 NO₂ Br CH₂C₆H₅ CH₂CH₂CH₃ A-416 NO₂Br CH₂C₆H₅ CH₂CH₂OCH₃ A-417 NO₂ CN CH₃ CH₃ A-418 NO₂ CN CH₃ CH₂CH₃ A-419NO₂ CN CH₃ CH₂CH₂CH₃ A-420 NO₂ CN CH₃ CH₂CH₂OCH₃ A-421 NO₂ CN CH₂CH₃ CH₃A-422 NO₂ CN CH₂CH₃ CH₂CH₃ A-423 NO₂ CN CH₂CH₃ CH₂CH₂CH₃ A-424 NO₂ CNCH₂CH₃ CH₂CH₂OCH₃ A-425 NO₂ CN CH₂OCH₃ CH₃ A-426 NO₂ CN CH₂OCH₃ CH₂CH₃A-427 NO₂ CN CH₂OCH₃ CH₂CH₂CH₃ A-428 NO₂ CN CH₂OCH₃ CH₂CH₂OCH₃ A-429 NO₂CN CH₂OCH₂CH₃ CH₃ A-430 NO₂ CN CH₂OCH₂CH₃ CH₂CH₃ A-431 NO₂ CN CH₂OCH₂CH₃CH₂CH₂CH₃ A-432 NO₂ CN CH₂OCH₂CH₃ CH₂CH₂OCH₃ A-433 NO₂ CN CH₂(CO)OCH₃CH₃ A-434 NO₂ CN CH₂(CO)OCH₃ CH₂CH₃ A-435 NO₂ CN CH₂(CO)OCH₃ CH₂CH₂CH₃A-436 NO₂ CN CH₂(CO)OCH₃ CH₂CH₂OCH₃ A-437 NO₂ CN CH₂CHCH₂ CH₃ A-438 NO₂CN CH₂CHCH₂ CH₂CH₃ A-439 NO₂ CN CH₂CHCH₂ CH₂CH₂CH₃ A-440 NO₂ CN CH₂CHCH₂CH₂CH₂OCH₃ A-441 NO₂ CN CH₂CCH CH₃ A-442 NO₂ CN CH₂CCH CH₂CH₃ A-443 NO₂CN CH₂CCH CH₂CH₂CH₃ A-444 NO₂ CN CH₂CCH CH₂CH₂OCH₃ A-445 NO₂ CN CH₂C₆H₅CH₃ A-446 NO₂ CN CH₂C₆H₅ CH₂CH₃ A-447 NO₂ CN CH₂C₆H₅ CH₂CH₂CH₃ A-448 NO₂CN CH₂C₆H₅ CH₂CH₂OCH₃ A-449 NO₂ CH₃ CH₃ CH₃ A-450 NO₂ CH₃ CH₃ CH₂CH₃A-451 NO₂ CH₃ CH₃ CH₂CH₂CH₃ A-452 NO₂ CH₃ CH₃ CH₂CH₂OCH₃ A-453 NO₂ CH₃CH₂CH₃ CH₃ A-454 NO₂ CH₃ CH₂CH₃ CH₂CH₃ A-455 NO₂ CH₃ CH₂CH₃ CH₂CH₂CH₃A-456 NO₂ CH₃ CH₂CH₃ CH₂CH₂OCH₃ A-457 NO₂ CH₃ CH₂OCH₃ CH₃ A-458 NO₂ CH₃CH₂OCH₃ CH₂CH₃ A-459 NO₂ CH₃ CH₂OCH₃ CH₂CH₂CH₃ A-460 NO₂ CH₃ CH₂OCH₃CH₂CH₂OCH₃ A-461 NO₂ CH₃ CH₂OCH₂CH₃ CH₃ A-462 NO₂ CH₃ CH₂OCH₂CH₃ CH₂CH₃A-463 NO₂ CH₃ CH₂OCH₂CH₃ CH₂CH₂CH₃ A-464 NO₂ CH₃ CH₂OCH₂CH₃ CH₂CH₂OCH₃A-465 NO₂ CH₃ CH₂(CO)OCH₃ CH₃ A-466 NO₂ CH₃ CH₂(CO)OCH₃ CH₂CH₃ A-467 NO₂CH₃ CH₂(CO)OCH₃ CH₂CH₂CH₃ A-468 NO₂ CH₃ CH₂(CO)OCH₃ CH₂CH₂OCH₃ A-469 NO₂CH₃ CH₂CHCH₂ CH₃ A-470 NO₂ CH₃ CH₂CHCH₂ CH₂CH₃ A-471 NO₂ CH₃ CH₂CHCH₂CH₂CH₂CH₃ A-472 NO₂ CH₃ CH₂CHCH₂ CH₂CH₂OCH₃ A-473 NO₂ CH₃ CH₂CCH CH₃A-474 NO₂ CH₃ CH₂CCH CH₂CH₃ A-475 NO₂ CH₃ CH₂CCH CH₂CH₂CH₃ A-476 NO₂ CH₃CH₂CCH CH₂CH₂OCH₃ A-477 NO₂ CH₃ CH₂C₆H₅ CH₃ A-478 NO₂ CH₃ CH₂C₆H₅ CH₂CH₃A-479 NO₂ CH₃ CH₂C₆H₅ CH₂CH₂CH₃ A-480 NO₂ CH₃ CH₂C₆H₅ CH₂CH₂OCH₃ A-481NO₂ CF₃ CH₃ CH₃ A-482 NO₂ CF₃ CH₃ CH₂CH₃ A-483 NO₂ CF₃ CH₃ CH₂CH₂CH₃A-484 NO₂ CF₃ CH₃ CH₂CH₂OCH₃ A-485 NO₂ CF₃ CH₂CH₃ CH₃ A-486 NO₂ CF₃CH₂CH₃ CH₂CH₃ A-487 NO₂ CF₃ CH₂CH₃ CH₂CH₂CH₃ A-488 NO₂ CF₃ CH₂CH₃CH₂CH₂OCH₃ A-489 NO₂ CF₃ CH₂OCH₃ CH₃ A-490 NO₂ CF₃ CH₂OCH₃ CH₂CH₃ A-491NO₂ CF₃ CH₂OCH₃ CH₂CH₂CH₃ A-492 NO₂ CF₃ CH₂OCH₃ CH₂CH₂OCH₃ A-493 NO₂ CF₃CH₂OCH₂CH₃ CH₃ A-494 NO₂ CF₃ CH₂OCH₂CH₃ CH₂CH₃ A-495 NO₂ CF₃ CH₂OCH₂CH₃CH₂CH₂CH₃ A-496 NO₂ CF₃ CH₂OCH₂CH₃ CH₂CH₂OCH₃ A-497 NO₂ CF₃ CH₂(CO)OCH₃CH₃ A-498 NO₂ CF₃ CH₂(CO)OCH₃ CH₂CH₃ A-499 NO₂ CF₃ CH₂(CO)OCH₃ CH₂CH₂CH₃A-500 NO₂ CF₃ CH₂(CO)OCH₃ CH₂CH₂OCH₃ A-501 NO₂ CF₃ CH₂CHCH₂ CH₃ A-502NO₂ CF₃ CH₂CHCH₂ CH₂CH₃ A-503 NO₂ CF₃ CH₂CHCH₂ CH₂CH₂CH₃ A-504 NO₂ CF₃CH₂CHCH₂ CH₂CH₂OCH₃ A-505 NO₂ CF₃ CH₂CCH CH₃ A-506 NO₂ CF₃ CH₂CCH CH₂CH₃A-507 NO₂ CF₃ CH₂CCH CH₂CH₂CH₃ A-508 NO₂ CF₃ CH₂CCH CH₂CH₂OCH₃ A-509 NO₂CF₃ CH₂C₆H₅ CH₃ A-510 NO₂ CF₃ CH₂C₆H₅ CH₂CH₃ A-511 NO₂ CF₃ CH₂C₆H₅CH₂CH₂CH₃ A-512 NO₂ CF₃ CH₂C₆H₅ CH₂CH₂OCH₃ A-513 NO₂ SO₂CH₃ CH₃ CH₃A-514 NO₂ SO₂CH₃ CH₃ CH₂CH₃ A-515 NO₂ SO₂CH₃ CH₃ CH₂CH₂CH₃ A-516 NO₂SO₂CH₃ CH₃ CH₂CH₂OCH₃ A-517 NO₂ SO₂CH₃ CH₂CH₃ CH₃ A-518 NO₂ SO₂CH₃CH₂CH₃ CH₂CH₃ A-519 NO₂ SO₂CH₃ CH₂CH₃ CH₂CH₂CH₃ A-520 NO₂ SO₂CH₃ CH₂CH₃CH₂CH₂OCH₃ A-521 NO₂ SO₂CH₃ CH₂OCH₃ CH₃ A-522 NO₂ SO₂CH₃ CH₂OCH₃ CH₂CH₃A-523 NO₂ SO₂CH₃ CH₂OCH₃ CH₂CH₂CH₃ A-524 NO₂ SO₂CH₃ CH₂OCH₃ CH₂CH₂OCH₃A-525 NO₂ SO₂CH₃ CH₂OCH₂CH₃ CH₃ A-526 NO₂ SO₂CH₃ CH₂OCH₂CH₃ CH₂CH₃ A-527NO₂ SO₂CH₃ CH₂OCH₂CH₃ CH₂CH₂CH₃ A-528 NO₂ SO₂CH₃ CH₂OCH₂CH₃ CH₂CH₂OCH₃A-529 NO₂ SO₂CH₃ CH₂(CO)OCH₃ CH₃ A-530 NO₂ SO₂CH₃ CH₂(CO)OCH₃ CH₂CH₃A-531 NO₂ SO₂CH₃ CH₂(CO)OCH₃ CH₂CH₂CH₃ A-532 NO₂ SO₂CH₃ CH₂(CO)OCH₃CH₂CH₂OCH₃ A-533 NO₂ SO₂CH₃ CH₂CHCH₂ CH₃ A-534 NO₂ SO₂CH₃ CH₂CHCH₂CH₂CH₃ A-535 NO₂ SO₂CH₃ CH₂CHCH₂ CH₂CH₂CH₃ A-536 NO₂ SO₂CH₃ CH₂CHCH₂CH₂CH₂OCH₃ A-537 NO₂ SO₂CH₃ CH₂CCH CH₃ A-538 NO₂ SO₂CH₃ CH₂CCH CH₂CH₃A-539 NO₂ SO₂CH₃ CH₂CCH CH₂CH₂CH₃ A-540 NO₂ SO₂CH₃ CH₂CCH CH₂CH₂OCH₃A-541 NO₂ SO₂CH₃ CH₂C₆H₅ CH₃ A-542 NO₂ SO₂CH₃ CH₂C₆H₅ CH₂CH₃ A-543 NO₂SO₂CH₃ CH₂C₆H₅ CH₂CH₂CH₃ A-544 NO₂ SO₂CH₃ CH₂C₆H₅ CH₂CH₂OCH₃ A-545 NO₂NO₂ CH₃ CH₃ A-546 NO₂ NO₂ CH₃ CH₂CH₃ A-547 NO₂ NO₂ CH₃ CH₂CH₂CH₃ A-548NO₂ NO₂ CH₃ CH₂CH₂OCH₃ A-549 NO₂ NO₂ CH₂CH₃ CH₃ A-550 NO₂ NO₂ CH₂CH₃CH₂CH₃ A-551 NO₂ NO₂ CH₂CH₃ CH₂CH₂CH₃ A-552 NO₂ NO₂ CH₂CH₃ CH₂CH₂OCH₃A-553 NO₂ NO₂ CH₂OCH₃ CH₃ A-554 NO₂ NO₂ CH₂OCH₃ CH₂CH₃ A-555 NO₂ NO₂CH₂OCH₃ CH₂CH₂CH₃ A-556 NO₂ NO₂ CH₂OCH₃ CH₂CH₂OCH₃ A-557 NO₂ NO₂CH₂OCH₂CH₃ CH₃ A-558 NO₂ NO₂ CH₂OCH₂CH₃ CH₂CH₃ A-559 NO₂ NO₂ CH₂OCH₂CH₃CH₂CH₂CH₃ A-560 NO₂ NO₂ CH₂OCH₂CH₃ CH₂CH₂OCH₃ A-561 NO₂ NO₂ CH₂(CO)OCH₃CH₃ A-562 NO₂ NO₂ CH₂(CO)OCH₃ CH₂CH₃ A-563 NO₂ NO₂ CH₂(CO)OCH₃ CH₂CH₂CH₃A-564 NO₂ NO₂ CH₂(CO)OCH₃ CH₂CH₂OCH₃ A-565 NO₂ NO₂ CH₂CHCH₂ CH₃ A-566NO₂ NO₂ CH₂CHCH₂ CH₂CH₃ A-567 NO₂ NO₂ CH₂CHCH₂ CH₂CH₂CH₃ A-568 NO₂ NO₂CH₂CHCH₂ CH₂CH₂OCH₃ A-569 NO₂ NO₂ CH₂CCH CH₃ A-570 NO₂ NO₂ CH₂CCH CH₂CH₃A-571 NO₂ NO₂ CH₂CCH CH₂CH₂CH₃ A-572 NO₂ NO₂ CH₂CCH CH₂CH₂OCH₃ A-573 NO₂NO₂ CH₂C₆H₅ CH₃ A-574 NO₂ NO₂ CH₂C₆H₅ CH₂CH₃ A-575 NO₂ NO₂ CH₂C₆H₅CH₂CH₂CH₃ A-576 NO₂ NO₂ CH₂C₆H₅ CH₂CH₂OCH₃ A-577 CH₃ H CH₃ CH₃ A-578 CH₃H CH₃ CH₂CH₃ A-579 CH₃ H CH₃ CH₂CH₂CH₃ A-580 CH₃ H CH₃ CH₂CH₂OCH₃ A-581CH₃ H CH₂CH₃ CH₃ A-582 CH₃ H CH₂CH₃ CH₂CH₃ A-583 CH₃ H CH₂CH₃ CH₂CH₂CH₃A-584 CH₃ H CH₂CH₃ CH₂CH₂OCH₃ A-585 CH₃ H CH₂OCH₃ CH₃ A-586 CH₃ HCH₂OCH₃ CH₂CH₃ A-587 CH₃ H CH₂OCH₃ CH₂CH₂CH₃ A-588 CH₃ H CH₂OCH₃CH₂CH₂OCH₃ A-589 CH₃ H CH₂OCH₂CH₃ CH₃ A-590 CH₃ H CH₂OCH₂CH₃ CH₂CH₃A-591 CH₃ H CH₂OCH₂CH₃ CH₂CH₂CH₃ A-592 CH₃ H CH₂OCH₂CH₃ CH₂CH₂OCH₃ A-593CH₃ H CH₂(CO)OCH₃ CH₃ A-594 CH₃ H CH₂(CO)OCH₃ CH₂CH₃ A-595 CH₃ HCH₂(CO)OCH₃ CH₂CH₂CH₃ A-596 CH₃ H CH₂(CO)OCH₃ CH₂CH₂OCH₃ A-597 CH₃ HCH₂CHCH₂ CH₃ A-598 CH₃ H CH₂CHCH₂ CH₂CH₃ A-599 CH₃ H CH₂CHCH₂ CH₂CH₂CH₃A-600 CH₃ H CH₂CHCH₂ CH₂CH₂OCH₃ A-601 CH₃ H CH₂CCH CH₃ A-602 CH₃ HCH₂CCH CH₂CH₃ A-603 CH₃ H CH₂CCH CH₂CH₂CH₃ A-604 CH₃ H CH₂CCH CH₂CH₂OCH₃A-605 CH₃ H CH₂C₆H₅ CH₃ A-606 CH₃ H CH₂C₆H₅ CH₂CH₃ A-607 CH₃ H CH₂C₆H₅CH₂CH₂CH₃ A-608 CH₃ H CH₂C₆H₅ CH₂CH₂OCH₃ A-609 CH₃ F CH₃ CH₃ A-610 CH₃ FCH₃ CH₂CH₃ A-611 CH₃ F CH₃ CH₂CH₂CH₃ A-612 CH₃ F CH₃ CH₂CH₂OCH₃ A-613CH₃ F CH₂CH₃ CH₃ A-614 CH₃ F CH₂CH₃ CH₂CH₃ A-615 CH₃ F CH₂CH₃ CH₂CH₂CH₃A-616 CH₃ F CH₂CH₃ CH₂CH₂OCH₃ A-617 CH₃ F CH₂OCH₃ CH₃ A-618 CH₃ FCH₂OCH₃ CH₂CH₃ A-619 CH₃ F CH₂OCH₃ CH₂CH₂CH₃ A-620 CH₃ F CH₂OCH₃CH₂CH₂OCH₃ A-621 CH₃ F CH₂OCH₂CH₃ CH₃ A-622 CH₃ F CH₂OCH₂CH₃ CH₂CH₃A-623 CH₃ F CH₂OCH₂CH₃ CH₂CH₂CH₃ A-624 CH₃ F CH₂OCH₂CH₃ CH₂CH₂OCH₃ A-625CH₃ F CH₂(CO)OCH₃ CH₃ A-626 CH₃ F CH₂(CO)OCH₃ CH₂CH₃ A-627 CH₃ FCH₂(CO)OCH₃ CH₂CH₂CH₃ A-628 CH₃ F CH₂(CO)OCH₃ CH₂CH₂OCH₃ A-629 CH₃ FCH₂CHCH₂ CH₃ A-630 CH₃ F CH₂CHCH₂ CH₂CH₃ A-631 CH₃ F CH₂CHCH₂ CH₂CH₂CH₃A-632 CH₃ F CH₂CHCH₂ CH₂CH₂OCH₃ A-633 CH₃ F CH₂CCH CH₃ A-634 CH₃ FCH₂CCH CH₂CH₃ A-635 CH₃ F CH₂CCH CH₂CH₂CH₃ A-636 CH₃ F CH₂CCH CH₂CH₂OCH₃A-637 CH₃ F CH₂C₆H₅ CH₃ A-638 CH₃ F CH₂C₆H₅ CH₂CH₃ A-639 CH₃ F CH₂C₆H₅CH₂CH₂CH₃ A-640 CH₃ F CH₂C₆H₅ CH₂CH₂OCH₃ A-641 CH₃ Cl CH₃ CH₃ A-642 CH₃Cl CH₃ CH₂CH₃ A-643 CH₃ Cl CH₃ CH₂CH₂CH₃ A-644 CH₃ Cl CH₃ CH₂CH₂OCH₃A-645 CH₃ Cl CH₂CH₃ CH₃ A-646 CH₃ Cl CH₂CH₃ CH₂CH₃ A-647 CH₃ Cl CH₂CH₃CH₂CH₂CH₃ A-648 CH₃ Cl CH₂CH₃ CH₂CH₂OCH₃ A-649 CH₃ Cl CH₂OCH₃ CH₃ A-650CH₃ Cl CH₂OCH₃ CH₂CH₃ A-651 CH₃ Cl CH₂OCH₃ CH₂CH₂CH₃ A-652 CH₃ ClCH₂OCH₃ CH₂CH₂OCH₃ A-653 CH₃ Cl CH₂OCH₂CH₃ CH₃ A-654 CH₃ Cl CH₂OCH₂CH₃CH₂CH₃ A-655 CH₃ Cl CH₂OCH₂CH₃ CH₂CH₂CH₃ A-656 CH₃ Cl CH₂OCH₂CH₃CH₂CH₂OCH₃ A-657 CH₃ Cl CH₂(CO)OCH₃ CH₃ A-658 CH₃ Cl CH₂(CO)OCH₃ CH₂CH₃A-659 CH₃ Cl CH₂(CO)OCH₃ CH₂CH₂CH₃ A-660 CH₃ Cl CH₂(CO)OCH₃ CH₂CH₂OCH₃A-661 CH₃ Cl CH₂CHCH₂ CH₃ A-662 CH₃ Cl CH₂CHCH₂ CH₂CH₃ A-663 CH₃ ClCH₂CHCH₂ CH₂CH₂CH₃ A-664 CH₃ Cl CH₂CHCH₂ CH₂CH₂OCH₃ A-665 CH₃ Cl CH₂CCHCH₃ A-666 CH₃ Cl CH₂CCH CH₂CH₃ A-667 CH₃ Cl CH₂CCH CH₂CH₂CH₃ A-668 CH₃Cl CH₂CCH CH₂CH₂OCH₃ A-669 CH₃ Cl CH₂C₆H₅ CH₃ A-670 CH₃ Cl CH₂C₆H₅CH₂CH₃ A-671 CH₃ Cl CH₂C₆H₅ CH₂CH₂CH₃ A-672 CH₃ Cl CH₂C₆H₅ CH₂CH₂OCH₃A-673 CH₃ Br CH₃ CH₃ A-674 CH₃ Br CH₃ CH₂CH₃ A-675 CH₃ Br CH₃ CH₂CH₂CH₃A-676 CH₃ Br CH₃ CH₂CH₂OCH₃ A-677 CH₃ Br CH₂CH₃ CH₃ A-678 CH₃ Br CH₂CH₃CH₂CH₃ A-679 CH₃ Br CH₂CH₃ CH₂CH₂CH₃ A-680 CH₃ Br CH₂CH₃ CH₂CH₂OCH₃A-681 CH₃ Br CH₂OCH₃ CH₃ A-682 CH₃ Br CH₂OCH₃ CH₂CH₃ A-683 CH₃ BrCH₂OCH₃ CH₂CH₂CH₃ A-684 CH₃ Br CH₂OCH₃ CH₂CH₂OCH₃ A-685 CH₃ BrCH₂OCH₂CH₃ CH₃ A-686 CH₃ Br CH₂OCH₂CH₃ CH₂CH₃ A-687 CH₃ Br CH₂OCH₂CH₃CH₂CH₂CH₃ A-688 CH₃ Br CH₂OCH₂CH₃ CH₂CH₂OCH₃ A-689 CH₃ Br CH₂(CO)OCH₃CH₃ A-690 CH₃ Br CH₂(CO)OCH₃ CH₂CH₃ A-691 CH₃ Br CH₂(CO)OCH₃ CH₂CH₂CH₃A-692 CH₃ Br CH₂(CO)OCH₃ CH₂CH₂OCH₃ A-693 CH₃ Br CH₂CHCH₂ CH₃ A-694 CH₃Br CH₂CHCH₂ CH₂CH₃ A-695 CH₃ Br CH₂CHCH₂ CH₂CH₂CH₃ A-696 CH₃ Br CH₂CHCH₂CH₂CH₂OCH₃ A-697 CH₃ Br CH₂CCH CH₃ A-698 CH₃ Br CH₂CCH CH₂CH₃ A-699 CH₃Br CH₂CCH CH₂CH₂CH₃ A-700 CH₃ Br CH₂CCH CH₂CH₂OCH₃ A-701 CH₃ Br CH₂C₆H₅CH₃ A-702 CH₃ Br CH₂C₆H₅ CH₂CH₃ A-703 CH₃ Br CH₂C₆H₅ CH₂CH₂CH₃ A-704 CH₃Br CH₂C₆H₅ CH₂CH₂OCH₃ A-705 CH₃ CN CH₃ CH₃ A-706 CH₃ CN CH₃ CH₂CH₃ A-707CH₃ CN CH₃ CH₂CH₂CH₃ A-708 CH₃ CN CH₃ CH₂CH₂OCH₃ A-709 CH₃ CN CH₂CH₃ CH₃A-710 CH₃ CN CH₂CH₃ CH₂CH₃ A-711 CH₃ CN CH₂CH₃ CH₂CH₂CH₃ A-712 CH₃ CNCH₂CH₃ CH₂CH₂OCH₃ A-713 CH₃ CN CH₂OCH₃ CH₃ A-714 CH₃ CN CH₂OCH₃ CH₂CH₃A-715 CH₃ CN CH₂OCH₃ CH₂CH₂CH₃ A-716 CH₃ CN CH₂OCH₃ CH₂CH₂OCH₃ A-717 CH₃CN CH₂OCH₂CH₃ CH₃ A-718 CH₃ CN CH₂OCH₂CH₃ CH₂CH₃ A-719 CH₃ CN CH₂OCH₂CH₃CH₂CH₂CH₃ A-720 CH₃ CN CH₂OCH₂CH₃ CH₂CH₂OCH₃ A-721 CH₃ CN CH₂(CO)OCH₃CH₃ A-722 CH₃ CN CH₂(CO)OCH₃ CH₂CH₃ A-723 CH₃ CN CH₂(CO)OCH₃ CH₂CH₂CH₃A-724 CH₃ CN CH₂(CO)OCH₃ CH₂CH₂OCH₃ A-725 CH₃ CN CH₂CHCH₂ CH₃ A-726 CH₃CN CH₂CHCH₂ CH₂CH₃ A-727 CH₃ CN CH₂CHCH₂ CH₂CH₂CH₃ A-728 CH₃ CN CH₂CHCH₂CH₂CH₂OCH₃ A-729 CH₃ CN CH₂CCH CH₃ A-730 CH₃ CN CH₂CCH CH₂CH₃ A-731 CH₃CN CH₂CCH CH₂CH₂CH₃ A-732 CH₃ CN CH₂CCH CH₂CH₂OCH₃ A-733 CH₃ CN CH₂C₆H₅CH₃ A-734 CH₃ CN CH₂C₆H₅ CH₂CH₃ A-735 CH₃ CN CH₂C₆H₅ CH₂CH₂CH₃ A-736 CH₃CN CH₂C₆H₅ CH₂CH₂OCH₃ A-737 CH₃ CH₃ CH₃ CH₃ A-738 CH₃ CH₃ CH₃ CH₂CH₃A-739 CH₃ CH₃ CH₃ CH₂CH₂CH₃ A-740 CH₃ CH₃ CH₃ CH₂CH₂OCH₃ A-741 CH₃ CH₃CH₂CH₃ CH₃ A-742 CH₃ CH₃ CH₂CH₃ CH₂CH₃ A-743 CH₃ CH₃ CH₂CH₃ CH₂CH₂CH₃A-744 CH₃ CH₃ CH₂CH₃ CH₂CH₂OCH₃ A-745 CH₃ CH₃ CH₂OCH₃ CH₃ A-746 CH₃ CH₃CH₂OCH₃ CH₂CH₃ A-747 CH₃ CH₃ CH₂OCH₃ CH₂CH₂CH₃ A-748 CH₃ CH₃ CH₂OCH₃CH₂CH₂OCH₃ A-749 CH₃ CH₃ CH₂OCH₂CH₃ CH₃ A-750 CH₃ CH₃ CH₂OCH₂CH₃ CH₂CH₃A-751 CH₃ CH₃ CH₂OCH₂CH₃ CH₂CH₂CH₃ A-752 CH₃ CH₃ CH₂OCH₂CH₃ CH₂CH₂OCH₃A-753 CH₃ CH₃ CH₂(CO)OCH₃ CH₃ A-754 CH₃ CH₃ CH₂(CO)OCH₃ CH₂CH₃ A-755 CH₃CH₃ CH₂(CO)OCH₃ CH₂CH₂CH₃ A-756 CH₃ CH₃ CH₂(CO)OCH₃ CH₂CH₂OCH₃ A-757 CH₃CH₃ CH₂CHCH₂ CH₃ A-758 CH₃ CH₃ CH₂CHCH₂ CH₂CH₃ A-759 CH₃ CH₃ CH₂CHCH₂CH₂CH₂CH₃ A-760 CH₃ CH₃ CH₂CHCH₂ CH₂CH₂OCH₃ A-761 CH₃ CH₃ CH₂CCH CH₃A-762 CH₃ CH₃ CH₂CCH CH₂CH₃ A-763 CH₃ CH₃ CH₂CCH CH₂CH₂CH₃ A-764 CH₃ CH₃CH₂CCH CH₂CH₂OCH₃ A-765 CH₃ CH₃ CH₂C₆H₅ CH₃ A-766 CH₃ CH₃ CH₂C₆H₅ CH₂CH₃A-767 CH₃ CH₃ CH₂C₆H₅ CH₂CH₂CH₃ A-768 CH₃ CH₃ CH₂C₆H₅ CH₂CH₂OCH₃ A-769CH₃ CF₃ CH₃ CH₃ A-770 CH₃ CF₃ CH₃ CH₂CH₃ A-771 CH₃ CF₃ CH₃ CH₂CH₂CH₃A-772 CH₃ CF₃ CH₃ CH₂CH₂OCH₃ A-773 CH₃ CF₃ CH₂CH₃ CH₃ A-774 CH₃ CF₃CH₂CH₃ CH₂CH₃ A-775 CH₃ CF₃ CH₂CH₃ CH₂CH₂CH₃ A-776 CH₃ CF₃ CH₂CH₃CH₂CH₂OCH₃ A-777 CH₃ CF₃ CH₂OCH₃ CH₃ A-778 CH₃ CF₃ CH₂OCH₃ CH₂CH₃ A-779CH₃ CF₃ CH₂OCH₃ CH₂CH₂CH₃ A-780 CH₃ CF₃ CH₂OCH₃ CH₂CH₂OCH₃ A-781 CH₃ CF₃CH₂OCH₂CH₃ CH₃ A-782 CH₃ CF₃ CH₂OCH₂CH₃ CH₂CH₃ A-783 CH₃ CF₃ CH₂OCH₂CH₃CH₂CH₂CH₃ A-784 CH₃ CF₃ CH₂OCH₂CH₃ CH₂CH₂OCH₃ A-785 CH₃ CF₃ CH₂(CO)OCH₃CH₃ A-786 CH₃ CF₃ CH₂(CO)OCH₃ CH₂CH₃ A-787 CH₃ CF₃ CH₂(CO)OCH₃ CH₂CH₂CH₃A-788 CH₃ CF₃ CH₂(CO)OCH₃ CH₂CH₂OCH₃ A-789 CH₃ CF₃ CH₂CHCH₂ CH₃ A-790CH₃ CF₃ CH₂CHCH₂ CH₂CH₃ A-791 CH₃ CF₃ CH₂CHCH₂ CH₂CH₂CH₃ A-792 CH₃ CF₃CH₂CHCH₂ CH₂CH₂OCH₃ A-793 CH₃ CF₃ CH₂CCH CH₃ A-794 CH₃ CF₃ CH₂CCH CH₂CH₃A-795 CH₃ CF₃ CH₂CCH CH₂CH₂CH₃ A-796 CH₃ CF₃ CH₂CCH CH₂CH₂OCH₃ A-797 CH₃CF₃ CH₂C₆H₅ CH₃ A-798 CH₃ CF₃ CH₂C₆H₅ CH₂CH₃ A-799 CH₃ CF₃ CH₂C₆H₅CH₂CH₂CH₃ A-800 CH₃ CF₃ CH₂C₆H₅ CH₂CH₂OCH₃ A-801 CH₃ SO₂CH₃ CH₃ CH₃A-802 CH₃ SO₂CH₃ CH₃ CH₂CH₃ A-803 CH₃ SO₂CH₃ CH₃ CH₂CH₂CH₃ A-804 CH₃SO₂CH₃ CH₃ CH₂CH₂OCH₃ A-805 CH₃ SO₂CH₃ CH₂CH₃ CH₃ A-806 CH₃ SO₂CH₃CH₂CH₃ CH₂CH₃ A-807 CH₃ SO₂CH₃ CH₂CH₃ CH₂CH₂CH₃ A-808 CH₃ SO₂CH₃ CH₂CH₃CH₂CH₂OCH₃ A-809 CH₃ SO₂CH₃ CH₂OCH₃ CH₃ A-810 CH₃ SO₂CH₃ CH₂OCH₃ CH₂CH₃A-811 CH₃ SO₂CH₃ CH₂OCH₃ CH₂CH₂CH₃ A-812 CH₃ SO₂CH₃ CH₂OCH₃ CH₂CH₂OCH₃A-813 CH₃ SO₂CH₃ CH₂OCH₂CH₃ CH₃ A-814 CH₃ SO₂CH₃ CH₂OCH₂CH₃ CH₂CH₃ A-815CH₃ SO₂CH₃ CH₂OCH₂CH₃ CH₂CH₂CH₃ A-816 CH₃ SO₂CH₃ CH₂OCH₂CH₃ CH₂CH₂OCH₃A-817 CH₃ SO₂CH₃ CH₂(CO)OCH₃ CH₃ A-818 CH₃ SO₂CH₃ CH₂(CO)OCH₃ CH₂CH₃A-819 CH₃ SO₂CH₃ CH₂(CO)OCH₃ CH₂CH₂CH₃ A-820 CH₃ SO₂CH₃ CH₂(CO)OCH₃CH₂CH₂OCH₃ A-821 CH₃ SO₂CH₃ CH₂CHCH₂ CH₃ A-822 CH₃ SO₂CH₃ CH₂CHCH₂CH₂CH₃ A-823 CH₃ SO₂CH₃ CH₂CHCH₂ CH₂CH₂CH₃ A-824 CH₃ SO₂CH₃ CH₂CHCH₂CH₂CH₂OCH₃ A-825 CH₃ SO₂CH₃ CH₂CCH CH₃ A-826 CH₃ SO₂CH₃ CH₂CCH CH₂CH₃A-827 CH₃ SO₂CH₃ CH₂CCH CH₂CH₂CH₃ A-828 CH₃ SO₂CH₃ CH₂CCH CH₂CH₂OCH₃A-829 CH₃ SO₂CH₃ CH₂C₆H₅ CH₃ A-830 CH₃ SO₂CH₃ CH₂C₆H₅ CH₂CH₃ A-831 CH₃SO₂CH₃ CH₂C₆H₅ CH₂CH₂CH₃ A-832 CH₃ SO₂CH₃ CH₂C₆H₅ CH₂CH₂OCH₃ A-833 CH₃NO₂ CH₃ CH₃ A-834 CH₃ NO₂ CH₃ CH₂CH₃ A-835 CH₃ NO₂ CH₃ CH₂CH₂CH₃ A-836CH₃ NO₂ CH₃ CH₂CH₂OCH₃ A-837 CH₃ NO₂ CH₂CH₃ CH₃ A-838 CH₃ NO₂ CH₂CH₃CH₂CH₃ A-839 CH₃ NO₂ CH₂CH₃ CH₂CH₂CH₃ A-840 CH₃ NO₂ CH₂CH₃ CH₂CH₂OCH₃A-841 CH₃ NO₂ CH₂OCH₃ CH₃ A-842 CH₃ NO₂ CH₂OCH₃ CH₂CH₃ A-843 CH₃ NO₂CH₂OCH₃ CH₂CH₂CH₃ A-844 CH₃ NO₂ CH₂OCH₃ CH₂CH₂OCH₃ A-845 CH₃ NO₂CH₂OCH₂CH₃ CH₃ A-846 CH₃ NO₂ CH₂OCH₂CH₃ CH₂CH₃ A-847 CH₃ NO₂ CH₂OCH₂CH₃CH₂CH₂CH₃ A-848 CH₃ NO₂ CH₂OCH₂CH₃ CH₂CH₂OCH₃ A-849 CH₃ NO₂ CH₂(CO)OCH₃CH₃ A-850 CH₃ NO₂ CH₂(CO)OCH₃ CH₂CH₃ A-851 CH₃ NO₂ CH₂(CO)OCH₃ CH₂CH₂CH₃A-852 CH₃ NO₂ CH₂(CO)OCH₃ CH₂CH₂OCH₃ A-853 CH₃ NO₂ CH₂CHCH₂ CH₃ A-854CH₃ NO₂ CH₂CHCH₂ CH₂CH₃ A-855 CH₃ NO₂ CH₂CHCH₂ CH₂CH₂CH₃ A-856 CH₃ NO₂CH₂CHCH₂ CH₂CH₂OCH₃ A-857 CH₃ NO₂ CH₂CCH CH₃ A-858 CH₃ NO₂ CH₂CCH CH₂CH₃A-859 CH₃ NO₂ CH₂CCH CH₂CH₂CH₃ A-860 CH₃ NO₂ CH₂CCH CH₂CH₂OCH₃ A-861 CH₃NO₂ CH₂C₆H₅ CH₃ A-862 CH₃ NO₂ CH₂C₆H₅ CH₂CH₃ A-863 CH₃ NO₂ CH₂C₆H₅CH₂CH₂CH₃ A-864 CH₃ NO₂ CH₂C₆H₅ CH₂CH₂OCH₃ A-865 cyclopropyl H CH₃ CH₃A-866 cyclopropyl H CH₃ CH₂CH₃ A-867 cyclopropyl H CH₃ CH₂CH₂CH₃ A-868cyclopropyl H CH₃ CH₂CH₂OCH₃ A-869 cyclopropyl H CH₂CH₃ CH₃ A-870cyclopropyl H CH₂CH₃ CH₂CH₃ A-871 cyclopropyl H CH₂CH₃ CH₂CH₂CH₃ A-872cyclopropyl H CH₂CH₃ CH₂CH₂OCH₃ A-873 cyclopropyl H CH₂OCH₃ CH₃ A-874cyclopropyl H CH₂OCH₃ CH₂CH₃ A-875 cyclopropyl H CH₂OCH₃ CH₂CH₂CH₃ A-876cyclopropyl H CH₂OCH₃ CH₂CH₂OCH₃ A-877 cyclopropyl H CH₂OCH₂CH₃ CH₃A-878 cyclopropyl H CH₂OCH₂CH₃ CH₂CH₃ A-879 cyclopropyl H CH₂OCH₂CH₃CH₂CH₂CH₃ A-880 cyclopropyl H CH₂OCH₂CH₃ CH₂CH₂OCH₃ A-881 cyclopropyl HCH₂(CO)OCH₃ CH₃ A-882 cyclopropyl H CH₂(CO)OCH₃ CH₂CH₃ A-883 cyclopropylH CH₂(CO)OCH₃ CH₂CH₂CH₃ A-884 cyclopropyl H CH₂(CO)OCH₃ CH₂CH₂OCH₃ A-885cyclopropyl H CH₂CHCH₂ CH₃ A-886 cyclopropyl H CH₂CHCH₂ CH₂CH₃ A-887cyclopropyl H CH₂CHCH₂ CH₂CH₂CH₃ A-888 cyclopropyl H CH₂CHCH₂ CH₂CH₂OCH₃A-889 cyclopropyl H CH₂CCH CH₃ A-890 cyclopropyl H CH₂CCH CH₂CH₃ A-891cyclopropyl H CH₂CCH CH₂CH₂CH₃ A-892 cyclopropyl H CH₂CCH CH₂CH₂OCH₃A-893 cyclopropyl H CH₂C₆H₅ CH₃ A-894 cyclopropyl H CH₂C₆H₅ CH₂CH₃ A-895cyclopropyl H CH₂C₆H₅ CH₂CH₂CH₃ A-896 cyclopropyl H CH₂C₆H₅ CH₂CH₂OCH₃A-897 cyclopropyl F CH₃ CH₃ A-898 cyclopropyl F CH₃ CH₂CH₃ A-899cyclopropyl F CH₃ CH₂CH₂CH₃ A-900 cyclopropyl F CH₃ CH₂CH₂OCH₃ A-901cyclopropyl F CH₂CH₃ CH₃ A-902 cyclopropyl F CH₂CH₃ CH₂CH₃ A-903cyclopropyl F CH₂CH₃ CH₂CH₂CH₃ A-904 cyclopropyl F CH₂CH₃ CH₂CH₂OCH₃A-905 cyclopropyl F CH₂OCH₃ CH₃ A-906 cyclopropyl F CH₂OCH₃ CH₂CH₃ A-907cyclopropyl F CH₂OCH₃ CH₂CH₂CH₃ A-908 cyclopropyl F CH₂OCH₃ CH₂CH₂OCH₃A-909 cyclopropyl F CH₂OCH₂CH₃ CH₃ A-910 cyclopropyl F CH₂OCH₂CH₃ CH₂CH₃A-911 cyclopropyl F CH₂OCH₂CH₃ CH₂CH₂CH₃ A-912 cyclopropyl F CH₂OCH₂CH₃CH₂CH₂OCH₃ A-913 cyclopropyl F CH₂(CO)OCH₃ CH₃ A-914 cyclopropyl FCH₂(CO)OCH₃ CH₂CH₃ A-915 cyclopropyl F CH₂(CO)OCH₃ CH₂CH₂CH₃ A-916cyclopropyl F CH₂(CO)OCH₃ CH₂CH₂OCH₃ A-917 cyclopropyl F CH₂CHCH₂ CH₃A-918 cyclopropyl F CH₂CHCH₂ CH₂CH₃ A-919 cyclopropyl F CH₂CHCH₂CH₂CH₂CH₃ A-920 cyclopropyl F CH₂CHCH₂ CH₂CH₂OCH₃ A-921 cyclopropyl FCH₂CCH CH₃ A-922 cyclopropyl F CH₂CCH CH₂CH₃ A-923 cyclopropyl F CH₂CCHCH₂CH₂CH₃ A-924 cyclopropyl F CH₂CCH CH₂CH₂OCH₃ A-925 cyclopropyl FCH₂C₆H₅ CH₃ A-926 cyclopropyl F CH₂C₆H₅ CH₂CH₃ A-927 cyclopropyl FCH₂C₆H₅ CH₂CH₂CH₃ A-928 cyclopropyl F CH₂C₆H₅ CH₂CH₂OCH₃ A-929cyclopropyl Cl CH₃ CH₃ A-930 cyclopropyl Cl CH₃ CH₂CH₃ A-931 cyclopropylCl CH₃ CH₂CH₂CH₃ A-932 cyclopropyl Cl CH₃ CH₂CH₂OCH₃ A-933 cyclopropylCl CH₂CH₃ CH₃ A-934 cyclopropyl Cl CH₂CH₃ CH₂CH₃ A-935 cyclopropyl ClCH₂CH₃ CH₂CH₂CH₃ A-936 cyclopropyl Cl CH₂CH₃ CH₂CH₂OCH₃ A-937cyclopropyl Cl CH₂OCH₃ CH₃ A-938 cyclopropyl Cl CH₂OCH₃ CH₂CH₃ A-939cyclopropyl Cl CH₂OCH₃ CH₂CH₂CH₃ A-940 cyclopropyl Cl CH₂OCH₃ CH₂CH₂OCH₃A-941 cyclopropyl Cl CH₂OCH₂CH₃ CH₃ A-942 cyclopropyl Cl CH₂OCH₂CH₃CH₂CH₃ A-943 cyclopropyl Cl CH₂OCH₂CH₃ CH₂CH₂CH₃ A-944 cyclopropyl ClCH₂OCH₂CH₃ CH₂CH₂OCH₃ A-945 cyclopropyl Cl CH₂(CO)OCH₃ CH₃ A-946cyclopropyl Cl CH₂(CO)OCH₃ CH₂CH₃ A-947 cyclopropyl Cl CH₂(CO)OCH₃CH₂CH₂CH₃ A-948 cyclopropyl Cl CH₂(CO)OCH₃ CH₂CH₂OCH₃ A-949 cyclopropylCl CH₂CHCH₂ CH₃ A-950 cyclopropyl Cl CH₂CHCH₂ CH₂CH₃ A-951 cyclopropylCl CH₂CHCH₂ CH₂CH₂CH₃ A-952 cyclopropyl Cl CH₂CHCH₂ CH₂CH₂OCH₃ A-953cyclopropyl Cl CH₂CCH CH₃ A-954 cyclopropyl Cl CH₂CCH CH₂CH₃ A-955cyclopropyl Cl CH₂CCH CH₂CH₂CH₃ A-956 cyclopropyl Cl CH₂CCH CH₂CH₂OCH₃A-957 cyclopropyl Cl CH₂C₆H₅ CH₃ A-958 cyclopropyl Cl CH₂C₆H₅ CH₂CH₃A-959 cyclopropyl Cl CH₂C₆H₅ CH₂CH₂CH₃ A-960 cyclopropyl Cl CH₂C₆H₅CH₂CH₂OCH₃ A-961 cyclopropyl Br CH₃ CH₃ A-962 cyclopropyl Br CH₃ CH₂CH₃A-963 cyclopropyl Br CH₃ CH₂CH₂CH₃ A-964 cyclopropyl Br CH₃ CH₂CH₂OCH₃A-965 cyclopropyl Br CH₂CH₃ CH₃ A-966 cyclopropyl Br CH₂CH₃ CH₂CH₃ A-967cyclopropyl Br CH₂CH₃ CH₂CH₂CH₃ A-968 cyclopropyl Br CH₂CH₃ CH₂CH₂OCH₃A-969 cyclopropyl Br CH₂OCH₃ CH₃ A-970 cyclopropyl Br CH₂OCH₃ CH₂CH₃A-971 cyclopropyl Br CH₂OCH₃ CH₂CH₂CH₃ A-972 cyclopropyl Br CH₂OCH₃CH₂CH₂OCH₃ A-973 cyclopropyl Br CH₂OCH₂CH₃ CH₃ A-974 cyclopropyl BrCH₂OCH₂CH₃ CH₂CH₃ A-975 cyclopropyl Br CH₂OCH₂CH₃ CH₂CH₂CH₃ A-976cyclopropyl Br CH₂OCH₂CH₃ CH₂CH₂OCH₃ A-977 cyclopropyl Br CH₂(CO)OCH₃CH₃ A-978 cyclopropyl Br CH₂(CO)OCH₃ CH₂CH₃ A-979 cyclopropyl BrCH₂(CO)OCH₃ CH₂CH₂CH₃ A-980 cyclopropyl Br CH₂(CO)OCH₃ CH₂CH₂OCH₃ A-981cyclopropyl Br CH₂CHCH₂ CH₃ A-982 cyclopropyl Br CH₂CHCH₂ CH₂CH₃ A-983cyclopropyl Br CH₂CHCH₂ CH₂CH₂CH₃ A-984 cyclopropyl Br CH₂CHCH₂CH₂CH₂OCH₃ A-985 cyclopropyl Br CH₂CCH CH₃ A-986 cyclopropyl Br CH₂CCHCH₂CH₃ A-987 cyclopropyl Br CH₂CCH CH₂CH₂CH₃ A-988 cyclopropyl Br CH₂CCHCH₂CH₂OCH₃ A-989 cyclopropyl Br CH₂C₆H₅ CH₃ A-990 cyclopropyl Br CH₂C₆H₅CH₂CH₃ A-991 cyclopropyl Br CH₂C₆H₅ CH₂CH₂CH₃ A-992 cyclopropyl BrCH₂C₆H₅ CH₂CH₂OCH₃ A-993 cyclopropyl CN CH₃ CH₃ A-994 cyclopropyl CN CH₃CH₂CH₃ A-995 cyclopropyl CN CH₃ CH₂CH₂CH₃ A-996 cyclopropyl CN CH₃CH₂CH₂OCH₃ A-997 cyclopropyl CN CH₂CH₃ CH₃ A-998 cyclopropyl CN CH₂CH₃CH₂CH₃ A-999 cyclopropyl CN CH₂CH₃ CH₂CH₂CH₃ A-1000 cyclopropyl CNCH₂CH₃ CH₂CH₂OCH₃ A-1001 cyclopropyl CN CH₂OCH₃ CH₃ A-1002 cyclopropylCN CH₂OCH₃ CH₂CH₃ A-1003 cyclopropyl CN CH₂OCH₃ CH₂CH₂CH₃ A-1004cyclopropyl CN CH₂OCH₃ CH₂CH₂OCH₃ A-1005 cyclopropyl CN CH₂OCH₂CH₃ CH₃A-1006 cyclopropyl CN CH₂OCH₂CH₃ CH₂CH₃ A-1007 cyclopropyl CN CH₂OCH₂CH₃CH₂CH₂CH₃ A-1008 cyclopropyl CN CH₂OCH₂CH₃ CH₂CH₂OCH₃ A-1009 cyclopropylCN CH₂(CO)OCH₃ CH₃ A-1010 cyclopropyl CN CH₂(CO)OCH₃ CH₂CH₃ A-1011cyclopropyl CN CH₂(CO)OCH₃ CH₂CH₂CH₃ A-1012 cyclopropyl CN CH₂(CO)OCH₃CH₂CH₂OCH₃ A-1013 cyclopropyl CN CH₂CHCH₂ CH₃ A-1014 cyclopropyl CNCH₂CHCH₂ CH₂CH₃ A-1015 cyclopropyl CN CH₂CHCH₂ CH₂CH₂CH₃ A-1016cyclopropyl CN CH₂CHCH₂ CH₂CH₂OCH₃ A-1017 cyclopropyl CN CH₂CCH CH₃A-1018 cyclopropyl CN CH₂CCH CH₂CH₃ A-1019 cyclopropyl CN CH₂CCHCH₂CH₂CH₃ A-1020 cyclopropyl CN CH₂CCH CH₂CH₂OCH₃ A-1021 cyclopropyl CNCH₂C₆H₅ CH₃ A-1022 cyclopropyl CN CH₂C₆H₅ CH₂CH₃ A-1023 cyclopropyl CNCH₂C₆H₅ CH₂CH₂CH₃ A-1024 cyclopropyl CN CH₂C₆H₅ CH₂CH₂OCH₃ A-1025cyclopropyl CH₃ CH₃ CH₃ A-1026 cyclopropyl CH₃ CH₃ CH₂CH₃ A-1027cyclopropyl CH₃ CH₃ CH₂CH₂CH₃ A-1028 cyclopropyl CH₃ CH₃ CH₂CH₂OCH₃A-1029 cyclopropyl CH₃ CH₂CH₃ CH₃ A-1030 cyclopropyl CH₃ CH₂CH₃ CH₂CH₃A-1031 cyclopropyl CH₃ CH₂CH₃ CH₂CH₂CH₃ A-1032 cyclopropyl CH₃ CH₂CH₃CH₂CH₂OCH₃ A-1033 cyclopropyl CH₃ CH₂OCH₃ CH₃ A-1034 cyclopropyl CH₃CH₂OCH₃ CH₂CH₃ A-1035 cyclopropyl CH₃ CH₂OCH₃ CH₂CH₂CH₃ A-1036cyclopropyl CH₃ CH₂OCH₃ CH₂CH₂OCH₃ A-1037 cyclopropyl CH₃ CH₂OCH₂CH₃ CH₃A-1038 cyclopropyl CH₃ CH₂OCH₂CH₃ CH₂CH₃ A-1039 cyclopropyl CH₃CH₂OCH₂CH₃ CH₂CH₂CH₃ A-1040 cyclopropyl CH₃ CH₂OCH₂CH₃ CH₂CH₂OCH₃ A-1041cyclopropyl CH₃ CH₂(CO)OCH₃ CH₃ A-1042 cyclopropyl CH₃ CH₂(CO)OCH₃CH₂CH₃ A-1043 cyclopropyl CH₃ CH₂(CO)OCH₃ CH₂CH₂CH₃ A-1044 cyclopropylCH₃ CH₂(CO)OCH₃ CH₂CH₂OCH₃ A-1045 cyclopropyl CH₃ CH₂CHCH₂ CH₃ A-1046cyclopropyl CH₃ CH₂CHCH₂ CH₂CH₃ A-1047 cyclopropyl CH₃ CH₂CHCH₂CH₂CH₂CH₃ A-1048 cyclopropyl CH₃ CH₂CHCH₂ CH₂CH₂OCH₃ A-1049 cyclopropylCH₃ CH₂CCH CH₃ A-1050 cyclopropyl CH₃ CH₂CCH CH₂CH₃ A-1051 cyclopropylCH₃ CH₂CCH CH₂CH₂CH₃ A-1052 cyclopropyl CH₃ CH₂CCH CH₂CH₂OCH₃ A-1053cyclopropyl CH₃ CH₂C₆H₅ CH₃ A-1054 cyclopropyl CH₃ CH₂C₆H₅ CH₂CH₃ A-1055cyclopropyl CH₃ CH₂C₆H₅ CH₂CH₂CH₃ A-1056 cyclopropyl CH₃ CH₂C₆H₅CH₂CH₂OCH₃ A-1057 cyclopropyl CF₃ CH₃ CH₃ A-1058 cyclopropyl CF₃ CH₃CH₂CH₃ A-1059 cyclopropyl CF₃ CH₃ CH₂CH₂CH₃ A-1060 cyclopropyl CF₃ CH₃CH₂CH₂OCH₃ A-1061 cyclopropyl CF₃ CH₂CH₃ CH₃ A-1062 cyclopropyl CF₃CH₂CH₃ CH₂CH₃ A-1063 cyclopropyl CF₃ CH₂CH₃ CH₂CH₂CH₃ A-1064 cyclopropylCF₃ CH₂CH₃ CH₂CH₂OCH₃ A-1065 cyclopropyl CF₃ CH₂OCH₃ CH₃ A-1066cyclopropyl CF₃ CH₂OCH₃ CH₂CH₃ A-1067 cyclopropyl CF₃ CH₂OCH₃ CH₂CH₂CH₃A-1068 cyclopropyl CF₃ CH₂OCH₃ CH₂CH₂OCH₃ A-1069 cyclopropyl CF₃CH₂OCH₂CH₃ CH₃ A-1070 cyclopropyl CF₃ CH₂OCH₂CH₃ CH₂CH₃ A-1071cyclopropyl CF₃ CH₂OCH₂CH₃ CH₂CH₂CH₃ A-1072 cyclopropyl CF₃ CH₂OCH₂CH₃CH₂CH₂OCH₃ A-1073 cyclopropyl CF₃ CH₂(CO)OCH₃ CH₃ A-1074 cyclopropyl CF₃CH₂(CO)OCH₃ CH₂CH₃ A-1075 cyclopropyl CF₃ CH₂(CO)OCH₃ CH₂CH₂CH₃ A-1076cyclopropyl CF₃ CH₂(CO)OCH₃ CH₂CH₂OCH₃ A-1077 cyclopropyl CF₃ CH₂CHCH₂CH₃ A-1078 cyclopropyl CF₃ CH₂CHCH₂ CH₂CH₃ A-1079 cyclopropyl CF₃CH₂CHCH₂ CH₂CH₂CH₃ A-1080 cyclopropyl CF₃ CH₂CHCH₂ CH₂CH₂OCH₃ A-1081cyclopropyl CF₃ CH₂CCH CH₃ A-1082 cyclopropyl CF₃ CH₂CCH CH₂CH₃ A-1083cyclopropyl CF₃ CH₂CCH CH₂CH₂CH₃ A-1084 cyclopropyl CF₃ CH₂CCHCH₂CH₂OCH₃ A-1085 cyclopropyl CF₃ CH₂C₆H₅ CH₃ A-1086 cyclopropyl CF₃CH₂C₆H₅ CH₂CH₃ A-1087 cyclopropyl CF₃ CH₂C₆H₅ CH₂CH₂CH₃ A-1088cyclopropyl CF₃ CH₂C₆H₅ CH₂CH₂OCH₃ A-1089 cyclopropyl SO₂CH₃ CH₃ CH₃A-1090 cyclopropyl SO₂CH₃ CH₃ CH₂CH₃ A-1091 cyclopropyl SO₂CH₃ CH₃CH₂CH₂CH₃ A-1092 cyclopropyl SO₂CH₃ CH₃ CH₂CH₂OCH₃ A-1093 cyclopropylSO₂CH₃ CH₂CH₃ CH₃ A-1094 cyclopropyl SO₂CH₃ CH₂CH₃ CH₂CH₃ A-1095cyclopropyl SO₂CH₃ CH₂CH₃ CH₂CH₂CH₃ A-1096 cyclopropyl SO₂CH₃ CH₂CH₃CH₂CH₂OCH₃ A-1097 cyclopropyl SO₂CH₃ CH₂OCH₃ CH₃ A-1098 cyclopropylSO₂CH₃ CH₂OCH₃ CH₂CH₃ A-1099 cyclopropyl SO₂CH₃ CH₂OCH₃ CH₂CH₂CH₃ A-1100cyclopropyl SO₂CH₃ CH₂OCH₃ CH₂CH₂OCH₃ A-1101 cyclopropyl SO₂CH₃CH₂OCH₂CH₃ CH₃ A-1102 cyclopropyl SO₂CH₃ CH₂OCH₂CH₃ CH₂CH₃ A-1103cyclopropyl SO₂CH₃ CH₂OCH₂CH₃ CH₂CH₂CH₃ A-1104 cyclopropyl SO₂CH₃CH₂OCH₂CH₃ CH₂CH₂OCH₃ A-1105 cyclopropyl SO₂CH₃ CH₂(CO)OCH₃ CH₃ A-1106cyclopropyl SO₂CH₃ CH₂(CO)OCH₃ CH₂CH₃ A-1107 cyclopropyl SO₂CH₃CH₂(CO)OCH₃ CH₂CH₂CH₃ A-1108 cyclopropyl SO₂CH₃ CH₂(CO)OCH₃ CH₂CH₂OCH₃A-1109 cyclopropyl SO₂CH₃ CH₂CHCH₂ CH₃ A-1110 cyclopropyl SO₂CH₃CH₂CHCH₂ CH₂CH₃ A-1111 cyclopropyl SO₂CH₃ CH₂CHCH₂ CH₂CH₂CH₃ A-1112cyclopropyl SO₂CH₃ CH₂CHCH₂ CH₂CH₂OCH₃ A-1113 cyclopropyl SO₂CH₃ CH₂CCHCH₃ A-1114 cyclopropyl SO₂CH₃ CH₂CCH CH₂CH₃ A-1115 cyclopropyl SO₂CH₃CH₂CCH CH₂CH₂CH₃ A-1116 cyclopropyl SO₂CH₃ CH₂CCH CH₂CH₂OCH₃ A-1117cyclopropyl SO₂CH₃ CH₂C₆H₅ CH₃ A-1118 cyclopropyl SO₂CH₃ CH₂C₆H₅ CH₂CH₃A-1119 cyclopropyl SO₂CH₃ CH₂C₆H₅ CH₂CH₂CH₃ A-1120 cyclopropyl SO₂CH₃CH₂C₆H₅ CH₂CH₂OCH₃ A-1121 cyclopropyl NO₂ CH₃ CH₃ A-1122 cyclopropyl NO₂CH₃ CH₂CH₃ A-1123 cyclopropyl NO₂ CH₃ CH₂CH₂CH₃ A-1124 cyclopropyl NO₂CH₃ CH₂CH₂OCH₃ A-1125 cyclopropyl NO₂ CH₂CH₃ CH₃ A-1126 cyclopropyl NO₂CH₂CH₃ CH₂CH₃ A-1127 cyclopropyl NO₂ CH₂CH₃ CH₂CH₂CH₃ A-1128 cyclopropylNO₂ CH₂CH₃ CH₂CH₂OCH₃ A-1129 cyclopropyl NO₂ CH₂OCH₃ CH₃ A-1130cyclopropyl NO₂ CH₂OCH₃ CH₂CH₃ A-1131 cyclopropyl NO₂ CH₂OCH₃ CH₂CH₂CH₃A-1132 cyclopropyl NO₂ CH₂OCH₃ CH₂CH₂OCH₃ A-1133 cyclopropyl NO₂CH₂OCH₂CH₃ CH₃ A-1134 cyclopropyl NO₂ CH₂OCH₂CH₃ CH₂CH₃ A-1135cyclopropyl NO₂ CH₂OCH₂CH₃ CH₂CH₂CH₃ A-1136 cyclopropyl NO₂ CH₂OCH₂CH₃CH₂CH₂OCH₃ A-1137 cyclopropyl NO₂ CH₂(CO)OCH₃ CH₃ A-1138 cyclopropyl NO₂CH₂(CO)OCH₃ CH₂CH₃ A-1139 cyclopropyl NO₂ CH₂(CO)OCH₃ CH₂CH₂CH₃ A-1140cyclopropyl NO₂ CH₂(CO)OCH₃ CH₂CH₂OCH₃ A-1141 cyclopropyl NO₂ CH₂CHCH₂CH₃ A-1142 cyclopropyl NO₂ CH₂CHCH₂ CH₂CH₃ A-1143 cyclopropyl NO₂CH₂CHCH₂ CH₂CH₂CH₃ A-1144 cyclopropyl NO₂ CH₂CHCH₂ CH₂CH₂OCH₃ A-1145cyclopropyl NO₂ CH₂CCH CH₃ A-1146 cyclopropyl NO₂ CH₂CCH CH₂CH₃ A-1147cyclopropyl NO₂ CH₂CCH CH₂CH₂CH₃ A-1148 cyclopropyl NO₂ CH₂CCHCH₂CH₂OCH₃ A-1149 cyclopropyl NO₂ CH₂C₆H₅ CH₃ A-1150 cyclopropyl NO₂CH₂C₆H₅ CH₂CH₃ A-1151 cyclopropyl NO₂ CH₂C₆H₅ CH₂CH₂CH₃ A-1152cyclopropyl NO₂ CH₂C₆H₅ CH₂CH₂OCH₃ A-1153 CH₂OCH₃ H CH₃ CH₃ A-1154CH₂OCH₃ H CH₃ CH₂CH₃ A-1155 CH₂OCH₃ H CH₃ CH₂CH₂CH₃ A-1156 CH₂OCH₃ H CH₃CH₂CH₂OCH₃ A-1157 CH₂OCH₃ H CH₂CH₃ CH₃ A-1158 CH₂OCH₃ H CH₂CH₃ CH₂CH₃A-1159 CH₂OCH₃ H CH₂CH₃ CH₂CH₂CH₃ A-1160 CH₂OCH₃ H CH₂CH₃ CH₂CH₂OCH₃A-1161 CH₂OCH₃ H CH₂OCH₃ CH₃ A-1162 CH₂OCH₃ H CH₂OCH₃ CH₂CH₃ A-1163CH₂OCH₃ H CH₂OCH₃ CH₂CH₂CH₃ A-1164 CH₂OCH₃ H CH₂OCH₃ CH₂CH₂OCH₃ A-1165CH₂OCH₃ H CH₂OCH₂CH₃ CH₃ A-1166 CH₂OCH₃ H CH₂OCH₂CH₃ CH₂CH₃ A-1167CH₂OCH₃ H CH₂OCH₂CH₃ CH₂CH₂CH₃ A-1168 CH₂OCH₃ H CH₂OCH₂CH₃ CH₂CH₂OCH₃A-1169 CH₂OCH₃ H CH₂(CO)OCH₃ CH₃ A-1170 CH₂OCH₃ H CH₂(CO)OCH₃ CH₂CH₃A-1171 CH₂OCH₃ H CH₂(CO)OCH₃ CH₂CH₂CH₃ A-1172 CH₂OCH₃ H CH₂(CO)OCH₃CH₂CH₂OCH₃ A-1173 CH₂OCH₃ H CH₂CHCH₂ CH₃ A-1174 CH₂OCH₃ H CH₂CHCH₂CH₂CH₃ A-1175 CH₂OCH₃ H CH₂CHCH₂ CH₂CH₂CH₃ A-1176 CH₂OCH₃ H CH₂CHCH₂CH₂CH₂OCH₃ A-1177 CH₂OCH₃ H CH₂CCH CH₃ A-1178 CH₂OCH₃ H CH₂CCH CH₂CH₃A-1179 CH₂OCH₃ H CH₂CCH CH₂CH₂CH₃ A-1180 CH₂OCH₃ H CH₂CCH CH₂CH₂OCH₃A-1181 CH₂OCH₃ H CH₂C₆H₅ CH₃ A-1182 CH₂OCH₃ H CH₂C₆H₅ CH₂CH₃ A-1183CH₂OCH₃ H CH₂C₆H₅ CH₂CH₂CH₃ A-1184 CH₂OCH₃ H CH₂C₆H₅ CH₂CH₂OCH₃ A-1185CH₂OCH₃ F CH₃ CH₃ A-1186 CH₂OCH₃ F CH₃ CH₂CH₃ A-1187 CH₂OCH₃ F CH₃CH₂CH₂CH₃ A-1188 CH₂OCH₃ F CH₃ CH₂CH₂OCH₃ A-1189 CH₂OCH₃ F CH₂CH₃ CH₃A-1190 CH₂OCH₃ F CH₂CH₃ CH₂CH₃ A-1191 CH₂OCH₃ F CH₂CH₃ CH₂CH₂CH₃ A-1192CH₂OCH₃ F CH₂CH₃ CH₂CH₂OCH₃ A-1193 CH₂OCH₃ F CH₂OCH₃ CH₃ A-1194 CH₂OCH₃F CH₂OCH₃ CH₂CH₃ A-1195 CH₂OCH₃ F CH₂OCH₃ CH₂CH₂CH₃ A-1196 CH₂OCH₃ FCH₂OCH₃ CH₂CH₂OCH₃ A-1197 CH₂OCH₃ F CH₂OCH₂CH₃ CH₃ A-1198 CH₂OCH₃ FCH₂OCH₂CH₃ CH₂CH₃ A-1199 CH₂OCH₃ F CH₂OCH₂CH₃ CH₂CH₂CH₃ A-1200 CH₂OCH₃ FCH₂OCH₂CH₃ CH₂CH₂OCH₃ A-1201 CH₂OCH₃ F CH₂(CO)OCH₃ CH₃ A-1202 CH₂OCH₃ FCH₂(CO)OCH₃ CH₂CH₃ A-1203 CH₂OCH₃ F CH₂(CO)OCH₃ CH₂CH₂CH₃ A-1204 CH₂OCH₃F CH₂(CO)OCH₃ CH₂CH₂OCH₃ A-1205 CH₂OCH₃ F CH₂CHCH₂ CH₃ A-1206 CH₂OCH₃ FCH₂CHCH₂ CH₂CH₃ A-1207 CH₂OCH₃ F CH₂CHCH₂ CH₂CH₂CH₃ A-1208 CH₂OCH₃ FCH₂CHCH₂ CH₂CH₂OCH₃ A-1209 CH₂OCH₃ F CH₂CCH CH₃ A-1210 CH₂OCH₃ F CH₂CCHCH₂CH₃ A-1211 CH₂OCH₃ F CH₂CCH CH₂CH₂CH₃ A-1212 CH₂OCH₃ F CH₂CCHCH₂CH₂OCH₃ A-1213 CH₂OCH₃ F CH₂C₆H₅ CH₃ A-1214 CH₂OCH₃ F CH₂C₆H₅ CH₂CH₃A-1215 CH₂OCH₃ F CH₂C₆H₅ CH₂CH₂CH₃ A-1216 CH₂OCH₃ F CH₂C₆H₅ CH₂CH₂OCH₃A-1217 CH₂OCH₃ Cl CH₃ CH₃ A-1218 CH₂OCH₃ Cl CH₃ CH₂CH₃ A-1219 CH₂OCH₃ ClCH₃ CH₂CH₂CH₃ A-1220 CH₂OCH₃ Cl CH₃ CH₂CH₂OCH₃ A-1221 CH₂OCH₃ Cl CH₂CH₃CH₃ A-1222 CH₂OCH₃ Cl CH₂CH₃ CH₂CH₃ A-1223 CH₂OCH₃ Cl CH₂CH₃ CH₂CH₂CH₃A-1224 CH₂OCH₃ Cl CH₂CH₃ CH₂CH₂OCH₃ A-1225 CH₂OCH₃ Cl CH₂OCH₃ CH₃ A-1226CH₂OCH₃ Cl CH₂OCH₃ CH₂CH₃ A-1227 CH₂OCH₃ Cl CH₂OCH₃ CH₂CH₂CH₃ A-1228CH₂OCH₃ Cl CH₂OCH₃ CH₂CH₂OCH₃ A-1229 CH₂OCH₃ Cl CH₂OCH₂CH₃ CH₃ A-1230CH₂OCH₃ Cl CH₂OCH₂CH₃ CH₂CH₃ A-1231 CH₂OCH₃ Cl CH₂OCH₂CH₃ CH₂CH₂CH₃A-1232 CH₂OCH₃ Cl CH₂OCH₂CH₃ CH₂CH₂OCH₃ A-1233 CH₂OCH₃ Cl CH₂(CO)OCH₃CH₃ A-1234 CH₂OCH₃ Cl CH₂(CO)OCH₃ CH₂CH₃ A-1235 CH₂OCH₃ Cl CH₂(CO)OCH₃CH₂CH₂CH₃ A-1236 CH₂OCH₃ Cl CH₂(CO)OCH₃ CH₂CH₂OCH₃ A-1237 CH₂OCH₃ ClCH₂CHCH₂ CH₃ A-1238 CH₂OCH₃ Cl CH₂CHCH₂ CH₂CH₃ A-1239 CH₂OCH₃ ClCH₂CHCH₂ CH₂CH₂CH₃ A-1240 CH₂OCH₃ Cl CH₂CHCH₂ CH₂CH₂OCH₃ A-1241 CH₂OCH₃Cl CH₂CCH CH₃ A-1242 CH₂OCH₃ Cl CH₂CCH CH₂CH₃ A-1243 CH₂OCH₃ Cl CH₂CCHCH₂CH₂CH₃ A-1244 CH₂OCH₃ Cl CH₂CCH CH₂CH₂OCH₃ A-1245 CH₂OCH₃ Cl CH₂C₆H₅CH₃ A-1246 CH₂OCH₃ Cl CH₂C₆H₅ CH₂CH₃ A-1247 CH₂OCH₃ Cl CH₂C₆H₅ CH₂CH₂CH₃A-1248 CH₂OCH₃ Cl CH₂C₆H₅ CH₂CH₂OCH₃ A-1249 CH₂OCH₃ Br CH₃ CH₃ A-1250CH₂OCH₃ Br CH₃ CH₂CH₃ A-1251 CH₂OCH₃ Br CH₃ CH₂CH₂CH₃ A-1252 CH₂OCH₃ BrCH₃ CH₂CH₂OCH₃ A-1253 CH₂OCH₃ Br CH₂CH₃ CH₃ A-1254 CH₂OCH₃ Br CH₂CH₃CH₂CH₃ A-1255 CH₂OCH₃ Br CH₂CH₃ CH₂CH₂CH₃ A-1256 CH₂OCH₃ Br CH₂CH₃CH₂CH₂OCH₃ A-1257 CH₂OCH₃ Br CH₂OCH₃ CH₃ A-1258 CH₂OCH₃ Br CH₂OCH₃CH₂CH₃ A-1259 CH₂OCH₃ Br CH₂OCH₃ CH₂CH₂CH₃ A-1260 CH₂OCH₃ Br CH₂OCH₃CH₂CH₂OCH₃ A-1261 CH₂OCH₃ Br CH₂OCH₂CH₃ CH₃ A-1262 CH₂OCH₃ Br CH₂OCH₂CH₃CH₂CH₃ A-1263 CH₂OCH₃ Br CH₂OCH₂CH₃ CH₂CH₂CH₃ A-1264 CH₂OCH₃ BrCH₂OCH₂CH₃ CH₂CH₂OCH₃ A-1265 CH₂OCH₃ Br CH₂(CO)OCH₃ CH₃ A-1266 CH₂OCH₃Br CH₂(CO)OCH₃ CH₂CH₃ A-1267 CH₂OCH₃ Br CH₂(CO)OCH₃ CH₂CH₂CH₃ A-1268CH₂OCH₃ Br CH₂(CO)OCH₃ CH₂CH₂OCH₃ A-1269 CH₂OCH₃ Br CH₂CHCH₂ CH₃ A-1270CH₂OCH₃ Br CH₂CHCH₂ CH₂CH₃ A-1271 CH₂OCH₃ Br CH₂CHCH₂ CH₂CH₂CH₃ A-1272CH₂OCH₃ Br CH₂CHCH₂ CH₂CH₂OCH₃ A-1273 CH₂OCH₃ Br CH₂CCH CH₃ A-1274CH₂OCH₃ Br CH₂CCH CH₂CH₃ A-1275 CH₂OCH₃ Br CH₂CCH CH₂CH₂CH₃ A-1276CH₂OCH₃ Br CH₂CCH CH₂CH₂OCH₃ A-1277 CH₂OCH₃ Br CH₂C₆H₅ CH₃ A-1278CH₂OCH₃ Br CH₂C₆H₅ CH₂CH₃ A-1279 CH₂OCH₃ Br CH₂C₆H₅ CH₂CH₂CH₃ A-1280CH₂OCH₃ Br CH₂C₆H₅ CH₂CH₂OCH₃ A-1281 CH₂OCH₃ CN CH₃ CH₃ A-1282 CH₂OCH₃CN CH₃ CH₂CH₃ A-1283 CH₂OCH₃ CN CH₃ CH₂CH₂CH₃ A-1284 CH₂OCH₃ CN CH₃CH₂CH₂OCH₃ A-1285 CH₂OCH₃ CN CH₂CH₃ CH₃ A-1286 CH₂OCH₃ CN CH₂CH₃ CH₂CH₃A-1287 CH₂OCH₃ CN CH₂CH₃ CH₂CH₂CH₃ A-1288 CH₂OCH₃ CN CH₂CH₃ CH₂CH₂OCH₃A-1289 CH₂OCH₃ CN CH₂OCH₃ CH₃ A-1290 CH₂OCH₃ CN CH₂OCH₃ CH₂CH₃ A-1291CH₂OCH₃ CN CH₂OCH₃ CH₂CH₂CH₃ A-1292 CH₂OCH₃ CN CH₂OCH₃ CH₂CH₂OCH₃ A-1293CH₂OCH₃ CN CH₂OCH₂CH₃ CH₃ A-1294 CH₂OCH₃ CN CH₂OCH₂CH₃ CH₂CH₃ A-1295CH₂OCH₃ CN CH₂OCH₂CH₃ CH₂CH₂CH₃ A-1296 CH₂OCH₃ CN CH₂OCH₂CH₃ CH₂CH₂OCH₃A-1297 CH₂OCH₃ CN CH₂(CO)OCH₃ CH₃ A-1298 CH₂OCH₃ CN CH₂(CO)OCH₃ CH₂CH₃A-1299 CH₂OCH₃ CN CH₂(CO)OCH₃ CH₂CH₂CH₃ A-1300 CH₂OCH₃ CN CH₂(CO)OCH₃CH₂CH₂OCH₃ A-1301 CH₂OCH₃ CN CH₂CHCH₂ CH₃ A-1302 CH₂OCH₃ CN CH₂CHCH₂CH₂CH₃ A-1303 CH₂OCH₃ CN CH₂CHCH₂ CH₂CH₂CH₃ A-1304 CH₂OCH₃ CN CH₂CHCH₂CH₂CH₂OCH₃ A-1305 CH₂OCH₃ CN CH₂CCH CH₃ A-1306 CH₂OCH₃ CN CH₂CCH CH₂CH₃A-1307 CH₂OCH₃ CN CH₂CCH CH₂CH₂CH₃ A-1308 CH₂OCH₃ CN CH₂CCH CH₂CH₂OCH₃A-1309 CH₂OCH₃ CN CH₂C₆H₅ CH₃ A-1310 CH₂OCH₃ CN CH₂C₆H₅ CH₂CH₃ A-1311CH₂OCH₃ CN CH₂C₆H₅ CH₂CH₂CH₃ A-1312 CH₂OCH₃ CN CH₂C₆H₅ CH₂CH₂OCH₃ A-1313CH₂OCH₃ CH₃ CH₃ CH₃ A-1314 CH₂OCH₃ CH₃ CH₃ CH₂CH₃ A-1315 CH₂OCH₃ CH₃ CH₃CH₂CH₂CH₃ A-1316 CH₂OCH₃ CH₃ CH₃ CH₂CH₂OCH₃ A-1317 CH₂OCH₃ CH₃ CH₂CH₃CH₃ A-1318 CH₂OCH₃ CH₃ CH₂CH₃ CH₂CH₃ A-1319 CH₂OCH₃ CH₃ CH₂CH₃ CH₂CH₂CH₃A-1320 CH₂OCH₃ CH₃ CH₂CH₃ CH₂CH₂OCH₃ A-1321 CH₂OCH₃ CH₃ CH₂OCH₃ CH₃A-1322 CH₂OCH₃ CH₃ CH₂OCH₃ CH₂CH₃ A-1323 CH₂OCH₃ CH₃ CH₂OCH₃ CH₂CH₂CH₃A-1324 CH₂OCH₃ CH₃ CH₂OCH₃ CH₂CH₂OCH₃ A-1325 CH₂OCH₃ CH₃ CH₂OCH₂CH₃ CH₃A-1326 CH₂OCH₃ CH₃ CH₂OCH₂CH₃ CH₂CH₃ A-1327 CH₂OCH₃ CH₃ CH₂OCH₂CH₃CH₂CH₂CH₃ A-1328 CH₂OCH₃ CH₃ CH₂OCH₂CH₃ CH₂CH₂OCH₃ A-1329 CH₂OCH₃ CH₃CH₂(CO)OCH₃ CH₃ A-1330 CH₂OCH₃ CH₃ CH₂(CO)OCH₃ CH₂CH₃ A-1331 CH₂OCH₃ CH₃CH₂(CO)OCH₃ CH₂CH₂CH₃ A-1332 CH₂OCH₃ CH₃ CH₂(CO)OCH₃ CH₂CH₂OCH₃ A-1333CH₂OCH₃ CH₃ CH₂CHCH₂ CH₃ A-1334 CH₂OCH₃ CH₃ CH₂CHCH₂ CH₂CH₃ A-1335CH₂OCH₃ CH₃ CH₂CHCH₂ CH₂CH₂CH₃ A-1336 CH₂OCH₃ CH₃ CH₂CHCH₂ CH₂CH₂OCH₃A-1337 CH₂OCH₃ CH₃ CH₂CCH CH₃ A-1338 CH₂OCH₃ CH₃ CH₂CCH CH₂CH₃ A-1339CH₂OCH₃ CH₃ CH₂CCH CH₂CH₂CH₃ A-1340 CH₂OCH₃ CH₃ CH₂CCH CH₂CH₂OCH₃ A-1341CH₂OCH₃ CH₃ CH₂C₆H₅ CH₃ A-1342 CH₂OCH₃ CH₃ CH₂C₆H₅ CH₂CH₃ A-1343 CH₂OCH₃CH₃ CH₂C₆H₅ CH₂CH₂CH₃ A-1344 CH₂OCH₃ CH₃ CH₂C₆H₅ CH₂CH₂OCH₃ A-1345CH₂OCH₃ CF₃ CH₃ CH₃ A-1346 CH₂OCH₃ CF₃ CH₃ CH₂CH₃ A-1347 CH₂OCH₃ CF₃ CH₃CH₂CH₂CH₃ A-1348 CH₂OCH₃ CF₃ CH₃ CH₂CH₂OCH₃ A-1349 CH₂OCH₃ CF₃ CH₂CH₃CH₃ A-1350 CH₂OCH₃ CF₃ CH₂CH₃ CH₂CH₃ A-1351 CH₂OCH₃ CF₃ CH₂CH₃ CH₂CH₂CH₃A-1352 CH₂OCH₃ CF₃ CH₂CH₃ CH₂CH₂OCH₃ A-1353 CH₂OCH₃ CF₃ CH₂OCH₃ CH₃A-1354 CH₂OCH₃ CF₃ CH₂OCH₃ CH₂CH₃ A-1355 CH₂OCH₃ CF₃ CH₂OCH₃ CH₂CH₂CH₃A-1356 CH₂OCH₃ CF₃ CH₂OCH₃ CH₂CH₂OCH₃ A-1357 CH₂OCH₃ CF₃ CH₂OCH₂CH₃ CH₃A-1358 CH₂OCH₃ CF₃ CH₂OCH₂CH₃ CH₂CH₃ A-1359 CH₂OCH₃ CF₃ CH₂OCH₂CH₃CH₂CH₂CH₃ A-1360 CH₂OCH₃ CF₃ CH₂OCH₂CH₃ CH₂CH₂OCH₃ A-1361 CH₂OCH₃ CF₃CH₂(CO)OCH₃ CH₃ A-1362 CH₂OCH₃ CF₃ CH₂(CO)OCH₃ CH₂CH₃ A-1363 CH₂OCH₃ CF₃CH₂(CO)OCH₃ CH₂CH₂CH₃ A-1364 CH₂OCH₃ CF₃ CH₂(CO)OCH₃ CH₂CH₂OCH₃ A-1365CH₂OCH₃ CF₃ CH₂CHCH₂ CH₃ A-1366 CH₂OCH₃ CF₃ CH₂CHCH₂ CH₂CH₃ A-1367CH₂OCH₃ CF₃ CH₂CHCH₂ CH₂CH₂CH₃ A-1368 CH₂OCH₃ CF₃ CH₂CHCH₂ CH₂CH₂OCH₃A-1369 CH₂OCH₃ CF₃ CH₂CCH CH₃ A-1370 CH₂OCH₃ CF₃ CH₂CCH CH₂CH₃ A-1371CH₂OCH₃ CF₃ CH₂CCH CH₂CH₂CH₃ A-1372 CH₂OCH₃ CF₃ CH₂CCH CH₂CH₂OCH₃ A-1373CH₂OCH₃ CF₃ CH₂C₆H₅ CH₃ A-1374 CH₂OCH₃ CF₃ CH₂C₆H₅ CH₂CH₃ A-1375 CH₂OCH₃CF₃ CH₂C₆H₅ CH₂CH₂CH₃ A-1376 CH₂OCH₃ CF₃ CH₂C₆H₅ CH₂CH₂OCH₃ A-1377CH₂OCH₃ SO₂CH₃ CH₃ CH₃ A-1378 CH₂OCH₃ SO₂CH₃ CH₃ CH₂CH₃ A-1379 CH₂OCH₃SO₂CH₃ CH₃ CH₂CH₂CH₃ A-1380 CH₂OCH₃ SO₂CH₃ CH₃ CH₂CH₂OCH₃ A-1381 CH₂OCH₃SO₂CH₃ CH₂CH₃ CH₃ A-1382 CH₂OCH₃ SO₂CH₃ CH₂CH₃ CH₂CH₃ A-1383 CH₂OCH₃SO₂CH₃ CH₂CH₃ CH₂CH₂CH₃ A-1384 CH₂OCH₃ SO₂CH₃ CH₂CH₃ CH₂CH₂OCH₃ A-1385CH₂OCH₃ SO₂CH₃ CH₂OCH₃ CH₃ A-1386 CH₂OCH₃ SO₂CH₃ CH₂OCH₃ CH₂CH₃ A-1387CH₂OCH₃ SO₂CH₃ CH₂OCH₃ CH₂CH₂CH₃ A-1388 CH₂OCH₃ SO₂CH₃ CH₂OCH₃CH₂CH₂OCH₃ A-1389 CH₂OCH₃ SO₂CH₃ CH₂OCH₂CH₃ CH₃ A-1390 CH₂OCH₃ SO₂CH₃CH₂OCH₂CH₃ CH₂CH₃ A-1391 CH₂OCH₃ SO₂CH₃ CH₂OCH₂CH₃ CH₂CH₂CH₃ A-1392CH₂OCH₃ SO₂CH₃ CH₂OCH₂CH₃ CH₂CH₂OCH₃ A-1393 CH₂OCH₃ SO₂CH₃ CH₂(CO)OCH₃CH₃ A-1394 CH₂OCH₃ SO₂CH₃ CH₂(CO)OCH₃ CH₂CH₃ A-1395 CH₂OCH₃ SO₂CH₃CH₂(CO)OCH₃ CH₂CH₂CH₃ A-1396 CH₂OCH₃ SO₂CH₃ CH₂(CO)OCH₃ CH₂CH₂OCH₃A-1397 CH₂OCH₃ SO₂CH₃ CH₂CHCH₂ CH₃ A-1398 CH₂OCH₃ SO₂CH₃ CH₂CHCH₂ CH₂CH₃A-1399 CH₂OCH₃ SO₂CH₃ CH₂CHCH₂ CH₂CH₂CH₃ A-1400 CH₂OCH₃ SO₂CH₃ CH₂CHCH₂CH₂CH₂OCH₃ A-1401 CH₂OCH₃ SO₂CH₃ CH₂CCH CH₃ A-1402 CH₂OCH₃ SO₂CH₃ CH₂CCHCH₂CH₃ A-1403 CH₂OCH₃ SO₂CH₃ CH₂CCH CH₂CH₂CH₃ A-1404 CH₂OCH₃ SO₂CH₃CH₂CCH CH₂CH₂OCH₃ A-1405 CH₂OCH₃ SO₂CH₃ CH₂C₆H₅ CH₃ A-1406 CH₂OCH₃SO₂CH₃ CH₂C₆H₅ CH₂CH₃ A-1407 CH₂OCH₃ SO₂CH₃ CH₂C₆H₅ CH₂CH₂CH₃ A-1408CH₂OCH₃ SO₂CH₃ CH₂C₆H₅ CH₂CH₂OCH₃ A-1409 CH₂OCH₃ NO₂ CH₃ CH₃ A-1410CH₂OCH₃ NO₂ CH₃ CH₂CH₃ A-1411 CH₂OCH₃ NO₂ CH₃ CH₂CH₂CH₃ A-1412 CH₂OCH₃NO₂ CH₃ CH₂CH₂OCH₃ A-1413 CH₂OCH₃ NO₂ CH₂CH₃ CH₃ A-1414 CH₂OCH₃ NO₂CH₂CH₃ CH₂CH₃ A-1415 CH₂OCH₃ NO₂ CH₂CH₃ CH₂CH₂CH₃ A-1416 CH₂OCH₃ NO₂CH₂CH₃ CH₂CH₂OCH₃ A-1417 CH₂OCH₃ NO₂ CH₂OCH₃ CH₃ A-1418 CH₂OCH₃ NO₂CH₂OCH₃ CH₂CH₃ A-1419 CH₂OCH₃ NO₂ CH₂OCH₃ CH₂CH₂CH₃ A-1420 CH₂OCH₃ NO₂CH₂OCH₃ CH₂CH₂OCH₃ A-1421 CH₂OCH₃ NO₂ CH₂OCH₂CH₃ CH₃ A-1422 CH₂OCH₃ NO₂CH₂OCH₂CH₃ CH₂CH₃ A-1423 CH₂OCH₃ NO₂ CH₂OCH₂CH₃ CH₂CH₂CH₃ A-1424 CH₂OCH₃NO₂ CH₂OCH₂CH₃ CH₂CH₂OCH₃ A-1425 CH₂OCH₃ NO₂ CH₂(CO)OCH₃ CH₃ A-1426CH₂OCH₃ NO₂ CH₂(CO)OCH₃ CH₂CH₃ A-1427 CH₂OCH₃ NO₂ CH₂(CO)OCH₃ CH₂CH₂CH₃A-1428 CH₂OCH₃ NO₂ CH₂(CO)OCH₃ CH₂CH₂OCH₃ A-1429 CH₂OCH₃ NO₂ CH₂CHCH₂CH₃ A-1430 CH₂OCH₃ NO₂ CH₂CHCH₂ CH₂CH₃ A-1431 CH₂OCH₃ NO₂ CH₂CHCH₂CH₂CH₂CH₃ A-1432 CH₂OCH₃ NO₂ CH₂CHCH₂ CH₂CH₂OCH₃ A-1433 CH₂OCH₃ NO₂CH₂CCH CH₃ A-1434 CH₂OCH₃ NO₂ CH₂CCH CH₂CH₃ A-1435 CH₂OCH₃ NO₂ CH₂CCHCH₂CH₂CH₃ A-1436 CH₂OCH₃ NO₂ CH₂CCH CH₂CH₂OCH₃ A-1437 CH₂OCH₃ NO₂CH₂C₆H₅ CH₃ A-1438 CH₂OCH₃ NO₂ CH₂C₆H₅ CH₂CH₃ A-1439 CH₂OCH₃ NO₂ CH₂C₆H₅CH₂CH₂CH₃ A-1440 CH₂OCH₃ NO₂ CH₂C₆H₅ CH₂CH₂OCH₃ A-1441 CH₂OCH₂CH₂OCH₃ HCH₃ CH₃ A-1442 CH₂OCH₂CH₂OCH₃ H CH₃ CH₂CH₃ A-1443 CH₂OCH₂CH₂OCH₃ H CH₃CH₂CH₂CH₃ A-1444 CH₂OCH₂CH₂OCH₃ H CH₃ CH₂CH₂OCH₃ A-1445 CH₂OCH₂CH₂OCH₃ HCH₂CH₃ CH₃ A-1446 CH₂OCH₂CH₂OCH₃ H CH₂CH₃ CH₂CH₃ A-1447 CH₂OCH₂CH₂OCH₃ HCH₂CH₃ CH₂CH₂CH₃ A-1448 CH₂OCH₂CH₂OCH₃ H CH₂CH₃ CH₂CH₂OCH₃ A-1449CH₂OCH₂CH₂OCH₃ H CH₂OCH₃ CH₃ A-1450 CH₂OCH₂CH₂OCH₃ H CH₂OCH₃ CH₂CH₃A-1451 CH₂OCH₂CH₂OCH₃ H CH₂OCH₃ CH₂CH₂CH₃ A-1452 CH₂OCH₂CH₂OCH₃ HCH₂OCH₃ CH₂CH₂OCH₃ A-1453 CH₂OCH₂CH₂OCH₃ H CH₂OCH₂CH₃ CH₃ A-1454CH₂OCH₂CH₂OCH₃ H CH₂OCH₂CH₃ CH₂CH₃ A-1455 CH₂OCH₂CH₂OCH₃ H CH₂OCH₂CH₃CH₂CH₂CH₃ A-1456 CH₂OCH₂CH₂OCH₃ H CH₂OCH₂CH₃ CH₂CH₂OCH₃ A-1457CH₂OCH₂CH₂OCH₃ H CH₂(CO)OCH₃ CH₃ A-1458 CH₂OCH₂CH₂OCH₃ H CH₂(CO)OCH₃CH₂CH₃ A-1459 CH₂OCH₂CH₂OCH₃ H CH₂(CO)OCH₃ CH₂CH₂CH₃ A-1460CH₂OCH₂CH₂OCH₃ H CH₂(CO)OCH₃ CH₂CH₂OCH₃ A-1461 CH₂OCH₂CH₂OCH₃ H CH₂CHCH₂CH₃ A-1462 CH₂OCH₂CH₂OCH₃ H CH₂CHCH₂ CH₂CH₃ A-1463 CH₂OCH₂CH₂OCH₃ HCH₂CHCH₂ CH₂CH₂CH₃ A-1464 CH₂OCH₂CH₂OCH₃ H CH₂CHCH₂ CH₂CH₂OCH₃ A-1465CH₂OCH₂CH₂OCH₃ H CH₂CCH CH₃ A-1466 CH₂OCH₂CH₂OCH₃ H CH₂CCH CH₂CH₃ A-1467CH₂OCH₂CH₂OCH₃ H CH₂CCH CH₂CH₂CH₃ A-1468 CH₂OCH₂CH₂OCH₃ H CH₂CCHCH₂CH₂OCH₃ A-1469 CH₂OCH₂CH₂OCH₃ H CH₂C₆H₅ CH₃ A-1470 CH₂OCH₂CH₂OCH₃ HCH₂C₆H₅ CH₂CH₃ A-1471 CH₂OCH₂CH₂OCH₃ H CH₂C₆H₅ CH₂CH₂CH₃ A-1472CH₂OCH₂CH₂OCH₃ H CH₂C₆H₅ CH₂CH₂OCH₃ A-1473 CH₂OCH₂CH₂OCH₃ F CH₃ CH₃A-1474 CH₂OCH₂CH₂OCH₃ F CH₃ CH₂CH₃ A-1475 CH₂OCH₂CH₂OCH₃ F CH₃ CH₂CH₂CH₃A-1476 CH₂OCH₂CH₂OCH₃ F CH₃ CH₂CH₂OCH₃ A-1477 CH₂OCH₂CH₂OCH₃ F CH₂CH₃CH₃ A-1478 CH₂OCH₂CH₂OCH₃ F CH₂CH₃ CH₂CH₃ A-1479 CH₂OCH₂CH₂OCH₃ F CH₂CH₃CH₂CH₂CH₃ A-1480 CH₂OCH₂CH₂OCH₃ F CH₂CH₃ CH₂CH₂OCH₃ A-1481CH₂OCH₂CH₂OCH₃ F CH₂OCH₃ CH₃ A-1482 CH₂OCH₂CH₂OCH₃ F CH₂OCH₃ CH₂CH₃A-1483 CH₂OCH₂CH₂OCH₃ F CH₂OCH₃ CH₂CH₂CH₃ A-1484 CH₂OCH₂CH₂OCH₃ FCH₂OCH₃ CH₂CH₂OCH₃ A-1485 CH₂OCH₂CH₂OCH₃ F CH₂OCH₂CH₃ CH₃ A-1486CH₂OCH₂CH₂OCH₃ F CH₂OCH₂CH₃ CH₂CH₃ A-1487 CH₂OCH₂CH₂OCH₃ F CH₂OCH₂CH₃CH₂CH₂CH₃ A-1488 CH₂OCH₂CH₂OCH₃ F CH₂OCH₂CH₃ CH₂CH₂OCH₃ A-1489CH₂OCH₂CH₂OCH₃ F CH₂(CO)OCH₃ CH₃ A-1490 CH₂OCH₂CH₂OCH₃ F CH₂(CO)OCH₃CH₂CH₃ A-1491 CH₂OCH₂CH₂OCH₃ F CH₂(CO)OCH₃ CH₂CH₂CH₃ A-1492CH₂OCH₂CH₂OCH₃ F CH₂(CO)OCH₃ CH₂CH₂OCH₃ A-1493 CH₂OCH₂CH₂OCH₃ F CH₂CHCH₂CH₃ A-1494 CH₂OCH₂CH₂OCH₃ F CH₂CHCH₂ CH₂CH₃ A-1495 CH₂OCH₂CH₂OCH₃ FCH₂CHCH₂ CH₂CH₂CH₃ A-1496 CH₂OCH₂CH₂OCH₃ F CH₂CHCH₂ CH₂CH₂OCH₃ A-1497CH₂OCH₂CH₂OCH₃ F CH₂CCH CH₃ A-1498 CH₂OCH₂CH₂OCH₃ F CH₂CCH CH₂CH₃ A-1499CH₂OCH₂CH₂OCH₃ F CH₂CCH CH₂CH₂CH₃ A-1500 CH₂OCH₂CH₂OCH₃ F CH₂CCHCH₂CH₂OCH₃ A-1501 CH₂OCH₂CH₂OCH₃ F CH₂C₆H₅ CH₃ A-1502 CH₂OCH₂CH₂OCH₃ FCH₂C₆H₅ CH₂CH₃ A-1503 CH₂OCH₂CH₂OCH₃ F CH₂C₆H₅ CH₂CH₂CH₃ A-1504CH₂OCH₂CH₂OCH₃ F CH₂C₆H₅ CH₂CH₂OCH₃ A-1505 CH₂OCH₂CH₂OCH₃ Cl CH₃ CH₃A-1506 CH₂OCH₂CH₂OCH₃ Cl CH₃ CH₂CH₃ A-1507 CH₂OCH₂CH₂OCH₃ Cl CH₃CH₂CH₂CH₃ A-1508 CH₂OCH₂CH₂OCH₃ Cl CH₃ CH₂CH₂OCH₃ A-1509 CH₂OCH₂CH₂OCH₃Cl CH₂CH₃ CH₃ A-1510 CH₂OCH₂CH₂OCH₃ Cl CH₂CH₃ CH₂CH₃ A-1511CH₂OCH₂CH₂OCH₃ Cl CH₂CH₃ CH₂CH₂CH₃ A-1512 CH₂OCH₂CH₂OCH₃ Cl CH₂CH₃CH₂CH₂OCH₃ A-1513 CH₂OCH₂CH₂OCH₃ Cl CH₂OCH₃ CH₃ A-1514 CH₂OCH₂CH₂OCH₃ ClCH₂OCH₃ CH₂CH₃ A-1515 CH₂OCH₂CH₂OCH₃ Cl CH₂OCH₃ CH₂CH₂CH₃ A-1516CH₂OCH₂CH₂OCH₃ Cl CH₂OCH₃ CH₂CH₂OCH₃ A-1517 CH₂OCH₂CH₂OCH₃ Cl CH₂OCH₂CH₃CH₃ A-1518 CH₂OCH₂CH₂OCH₃ Cl CH₂OCH₂CH₃ CH₂CH₃ A-1519 CH₂OCH₂CH₂OCH₃ ClCH₂OCH₂CH₃ CH₂CH₂CH₃ A-1520 CH₂OCH₂CH₂OCH₃ Cl CH₂OCH₂CH₃ CH₂CH₂OCH₃A-1521 CH₂OCH₂CH₂OCH₃ Cl CH₂(CO)OCH₃ CH₃ A-1522 CH₂OCH₂CH₂OCH₃ ClCH₂(CO)OCH₃ CH₂CH₃ A-1523 CH₂OCH₂CH₂OCH₃ Cl CH₂(CO)OCH₃ CH₂CH₂CH₃ A-1524CH₂OCH₂CH₂OCH₃ Cl CH₂(CO)OCH₃ CH₂CH₂OCH₃ A-1525 CH₂OCH₂CH₂OCH₃ ClCH₂CHCH₂ CH₃ A-1526 CH₂OCH₂CH₂OCH₃ Cl CH₂CHCH₂ CH₂CH₃ A-1527CH₂OCH₂CH₂OCH₃ Cl CH₂CHCH₂ CH₂CH₂CH₃ A-1528 CH₂OCH₂CH₂OCH₃ Cl CH₂CHCH₂CH₂CH₂OCH₃ A-1529 CH₂OCH₂CH₂OCH₃ Cl CH₂CCH CH₃ A-1530 CH₂OCH₂CH₂OCH₃ ClCH₂CCH CH₂CH₃ A-1531 CH₂OCH₂CH₂OCH₃ Cl CH₂CCH CH₂CH₂CH₃ A-1532CH₂OCH₂CH₂OCH₃ Cl CH₂CCH CH₂CH₂OCH₃ A-1533 CH₂OCH₂CH₂OCH₃ Cl CH₂C₆H₅ CH₃A-1534 CH₂OCH₂CH₂OCH₃ Cl CH₂C₆H₅ CH₂CH₃ A-1535 CH₂OCH₂CH₂OCH₃ Cl CH₂C₆H₅CH₂CH₂CH₃ A-1536 CH₂OCH₂CH₂OCH₃ Cl CH₂C₆H₅ CH₂CH₂OCH₃ A-1537CH₂OCH₂CH₂OCH₃ Br CH₃ CH₃ A-1538 CH₂OCH₂CH₂OCH₃ Br CH₃ CH₂CH₃ A-1539CH₂OCH₂CH₂OCH₃ Br CH₃ CH₂CH₂CH₃ A-1540 CH₂OCH₂CH₂OCH₃ Br CH₃ CH₂CH₂OCH₃A-1541 CH₂OCH₂CH₂OCH₃ Br CH₂CH₃ CH₃ A-1542 CH₂OCH₂CH₂OCH₃ Br CH₂CH₃CH₂CH₃ A-1543 CH₂OCH₂CH₂OCH₃ Br CH₂CH₃ CH₂CH₂CH₃ A-1544 CH₂OCH₂CH₂OCH₃Br CH₂CH₃ CH₂CH₂OCH₃ A-1545 CH₂OCH₂CH₂OCH₃ Br CH₂OCH₃ CH₃ A-1546CH₂OCH₂CH₂OCH₃ Br CH₂OCH₃ CH₂CH₃ A-1547 CH₂OCH₂CH₂OCH₃ Br CH₂OCH₃CH₂CH₂CH₃ A-1548 CH₂OCH₂CH₂OCH₃ Br CH₂OCH₃ CH₂CH₂OCH₃ A-1549CH₂OCH₂CH₂OCH₃ Br CH₂OCH₂CH₃ CH₃ A-1550 CH₂OCH₂CH₂OCH₃ Br CH₂OCH₂CH₃CH₂CH₃ A-1551 CH₂OCH₂CH₂OCH₃ Br CH₂OCH₂CH₃ CH₂CH₂CH₃ A-1552CH₂OCH₂CH₂OCH₃ Br CH₂OCH₂CH₃ CH₂CH₂OCH₃ A-1553 CH₂OCH₂CH₂OCH₃ BrCH₂(CO)OCH₃ CH₃ A-1554 CH₂OCH₂CH₂OCH₃ Br CH₂(CO)OCH₃ CH₂CH₃ A-1555CH₂OCH₂CH₂OCH₃ Br CH₂(CO)OCH₃ CH₂CH₂CH₃ A-1556 CH₂OCH₂CH₂OCH₃ BrCH₂(CO)OCH₃ CH₂CH₂OCH₃ A-1557 CH₂OCH₂CH₂OCH₃ Br CH₂CHCH₂ CH₃ A-1558CH₂OCH₂CH₂OCH₃ Br CH₂CHCH₂ CH₂CH₃ A-1559 CH₂OCH₂CH₂OCH₃ Br CH₂CHCH₂CH₂CH₂CH₃ A-1560 CH₂OCH₂CH₂OCH₃ Br CH₂CHCH₂ CH₂CH₂OCH₃ A-1561CH₂OCH₂CH₂OCH₃ Br CH₂CCH CH₃ A-1562 CH₂OCH₂CH₂OCH₃ Br CH₂CCH CH₂CH₃A-1563 CH₂OCH₂CH₂OCH₃ Br CH₂CCH CH₂CH₂CH₃ A-1564 CH₂OCH₂CH₂OCH₃ BrCH₂CCH CH₂CH₂OCH₃ A-1565 CH₂OCH₂CH₂OCH₃ Br CH₂C₆H₅ CH₃ A-1566CH₂OCH₂CH₂OCH₃ Br CH₂C₆H₅ CH₂CH₃ A-1567 CH₂OCH₂CH₂OCH₃ Br CH₂C₆H₅CH₂CH₂CH₃ A-1568 CH₂OCH₂CH₂OCH₃ Br CH₂C₆H₅ CH₂CH₂OCH₃ A-1569CH₂OCH₂CH₂OCH₃ CN CH₃ CH₃ A-1570 CH₂OCH₂CH₂OCH₃ CN CH₃ CH₂CH₃ A-1571CH₂OCH₂CH₂OCH₃ CN CH₃ CH₂CH₂CH₃ A-1572 CH₂OCH₂CH₂OCH₃ CN CH₃ CH₂CH₂OCH₃A-1573 CH₂OCH₂CH₂OCH₃ CN CH₂CH₃ CH₃ A-1574 CH₂OCH₂CH₂OCH₃ CN CH₂CH₃CH₂CH₃ A-1575 CH₂OCH₂CH₂OCH₃ CN CH₂CH₃ CH₂CH₂CH₃ A-1576 CH₂OCH₂CH₂OCH₃CN CH₂CH₃ CH₂CH₂OCH₃ A-1577 CH₂OCH₂CH₂OCH₃ CN CH₂OCH₃ CH₃ A-1578CH₂OCH₂CH₂OCH₃ CN CH₂OCH₃ CH₂CH₃ A-1579 CH₂OCH₂CH₂OCH₃ CN CH₂OCH₃CH₂CH₂CH₃ A-1580 CH₂OCH₂CH₂OCH₃ CN CH₂OCH₃ CH₂CH₂OCH₃ A-1581CH₂OCH₂CH₂OCH₃ CN CH₂OCH₂CH₃ CH₃ A-1582 CH₂OCH₂CH₂OCH₃ CN CH₂OCH₂CH₃CH₂CH₃ A-1583 CH₂OCH₂CH₂OCH₃ CN CH₂OCH₂CH₃ CH₂CH₂CH₃ A-1584CH₂OCH₂CH₂OCH₃ CN CH₂OCH₂CH₃ CH₂CH₂OCH₃ A-1585 CH₂OCH₂CH₂OCH₃ CNCH₂(CO)OCH₃ CH₃ A-1586 CH₂OCH₂CH₂OCH₃ CN CH₂(CO)OCH₃ CH₂CH₃ A-1587CH₂OCH₂CH₂OCH₃ CN CH₂(CO)OCH₃ CH₂CH₂CH₃ A-1588 CH₂OCH₂CH₂OCH₃ CNCH₂(CO)OCH₃ CH₂CH₂OCH₃ A-1589 CH₂OCH₂CH₂OCH₃ CN CH₂CHCH₂ CH₃ A-1590CH₂OCH₂CH₂OCH₃ CN CH₂CHCH₂ CH₂CH₃ A-1591 CH₂OCH₂CH₂OCH₃ CN CH₂CHCH₂CH₂CH₂CH₃ A-1592 CH₂OCH₂CH₂OCH₃ CN CH₂CHCH₂ CH₂CH₂OCH₃ A-1593CH₂OCH₂CH₂OCH₃ CN CH₂CCH CH₃ A-1594 CH₂OCH₂CH₂OCH₃ CN CH₂CCH CH₂CH₃A-1595 CH₂OCH₂CH₂OCH₃ CN CH₂CCH CH₂CH₂CH₃ A-1596 CH₂OCH₂CH₂OCH₃ CNCH₂CCH CH₂CH₂OCH₃ A-1597 CH₂OCH₂CH₂OCH₃ CN CH₂C₆H₅ CH₃ A-1598CH₂OCH₂CH₂OCH₃ CN CH₂C₆H₅ CH₂CH₃ A-1599 CH₂OCH₂CH₂OCH₃ CN CH₂C₆H₅CH₂CH₂CH₃ A-1600 CH₂OCH₂CH₂OCH₃ CN CH₂C₆H₅ CH₂CH₂OCH₃ A-1601CH₂OCH₂CH₂OCH₃ CH₃ CH₃ CH₃ A-1602 CH₂OCH₂CH₂OCH₃ CH₃ CH₃ CH₂CH₃ A-1603CH₂OCH₂CH₂OCH₃ CH₃ CH₃ CH₂CH₂CH₃ A-1604 CH₂OCH₂CH₂OCH₃ CH₃ CH₃CH₂CH₂OCH₃ A-1605 CH₂OCH₂CH₂OCH₃ CH₃ CH₂CH₃ CH₃ A-1606 CH₂OCH₂CH₂OCH₃CH₃ CH₂CH₃ CH₂CH₃ A-1607 CH₂OCH₂CH₂OCH₃ CH₃ CH₂CH₃ CH₂CH₂CH₃ A-1608CH₂OCH₂CH₂OCH₃ CH₃ CH₂CH₃ CH₂CH₂OCH₃ A-1609 CH₂OCH₂CH₂OCH₃ CH₃ CH₂OCH₃CH₃ A-1610 CH₂OCH₂CH₂OCH₃ CH₃ CH₂OCH₃ CH₂CH₃ A-1611 CH₂OCH₂CH₂OCH₃ CH₃CH₂OCH₃ CH₂CH₂CH₃ A-1612 CH₂OCH₂CH₂OCH₃ CH₃ CH₂OCH₃ CH₂CH₂OCH₃ A-1613CH₂OCH₂CH₂OCH₃ CH₃ CH₂OCH₂CH₃ CH₃ A-1614 CH₂OCH₂CH₂OCH₃ CH₃ CH₂OCH₂CH₃CH₂CH₃ A-1615 CH₂OCH₂CH₂OCH₃ CH₃ CH₂OCH₂CH₃ CH₂CH₂CH₃ A-1616CH₂OCH₂CH₂OCH₃ CH₃ CH₂OCH₂CH₃ CH₂CH₂OCH₃ A-1617 CH₂OCH₂CH₂OCH₃ CH₃CH₂(CO)OCH₃ CH₃ A-1618 CH₂OCH₂CH₂OCH₃ CH₃ CH₂(CO)OCH₃ CH₂CH₃ A-1619CH₂OCH₂CH₂OCH₃ CH₃ CH₂(CO)OCH₃ CH₂CH₂CH₃ A-1620 CH₂OCH₂CH₂OCH₃ CH₃CH₂(CO)OCH₃ CH₂CH₂OCH₃ A-1621 CH₂OCH₂CH₂OCH₃ CH₃ CH₂CHCH₂ CH₃ A-1622CH₂OCH₂CH₂OCH₃ CH₃ CH₂CHCH₂ CH₂CH₃ A-1623 CH₂OCH₂CH₂OCH₃ CH₃ CH₂CHCH₂CH₂CH₂CH₃ A-1624 CH₂OCH₂CH₂OCH₃ CH₃ CH₂CHCH₂ CH₂CH₂OCH₃ A-1625CH₂OCH₂CH₂OCH₃ CH₃ CH₂CCH CH₃ A-1626 CH₂OCH₂CH₂OCH₃ CH₃ CH₂CCH CH₂CH₃A-1627 CH₂OCH₂CH₂OCH₃ CH₃ CH₂CCH CH₂CH₂CH₃ A-1628 CH₂OCH₂CH₂OCH₃ CH₃CH₂CCH CH₂CH₂OCH₃ A-1629 CH₂OCH₂CH₂OCH₃ CH₃ CH₂C₆H₅ CH₃ A-1630CH₂OCH₂CH₂OCH₃ CH₃ CH₂C₆H₅ CH₂CH₃ A-1631 CH₂OCH₂CH₂OCH₃ CH₃ CH₂C₆H₅CH₂CH₂CH₃ A-1632 CH₂OCH₂CH₂OCH₃ CH₃ CH₂C₆H₅ CH₂CH₂OCH₃ A-1633CH₂OCH₂CH₂OCH₃ CF₃ CH₃ CH₃ A-1634 CH₂OCH₂CH₂OCH₃ CF₃ CH₃ CH₂CH₃ A-1635CH₂OCH₂CH₂OCH₃ CF₃ CH₃ CH₂CH₂CH₃ A-1636 CH₂OCH₂CH₂OCH₃ CF₃ CH₃CH₂CH₂OCH₃ A-1637 CH₂OCH₂CH₂OCH₃ CF₃ CH₂CH₃ CH₃ A-1638 CH₂OCH₂CH₂OCH₃CF₃ CH₂CH₃ CH₂CH₃ A-1639 CH₂OCH₂CH₂OCH₃ CF₃ CH₂CH₃ CH₂CH₂CH₃ A-1640CH₂OCH₂CH₂OCH₃ CF₃ CH₂CH₃ CH₂CH₂OCH₃ A-1641 CH₂OCH₂CH₂OCH₃ CF₃ CH₂OCH₃CH₃ A-1642 CH₂OCH₂CH₂OCH₃ CF₃ CH₂OCH₃ CH₂CH₃ A-1643 CH₂OCH₂CH₂OCH₃ CF₃CH₂OCH₃ CH₂CH₂CH₃ A-1644 CH₂OCH₂CH₂OCH₃ CF₃ CH₂OCH₃ CH₂CH₂OCH₃ A-1645CH₂OCH₂CH₂OCH₃ CF₃ CH₂OCH₂CH₃ CH₃ A-1646 CH₂OCH₂CH₂OCH₃ CF₃ CH₂OCH₂CH₃CH₂CH₃ A-1647 CH₂OCH₂CH₂OCH₃ CF₃ CH₂OCH₂CH₃ CH₂CH₂CH₃ A-1648CH₂OCH₂CH₂OCH₃ CF₃ CH₂OCH₂CH₃ CH₂CH₂OCH₃ A-1649 CH₂OCH₂CH₂OCH₃ CF₃CH₂(CO)OCH₃ CH₃ A-1650 CH₂OCH₂CH₂OCH₃ CF₃ CH₂(CO)OCH₃ CH₂CH₃ A-1651CH₂OCH₂CH₂OCH₃ CF₃ CH₂(CO)OCH₃ CH₂CH₂CH₃ A-1652 CH₂OCH₂CH₂OCH₃ CF₃CH₂(CO)OCH₃ CH₂CH₂OCH₃ A-1653 CH₂OCH₂CH₂OCH₃ CF₃ CH₂CHCH₂ CH₃ A-1654CH₂OCH₂CH₂OCH₃ CF₃ CH₂CHCH₂ CH₂CH₃ A-1655 CH₂OCH₂CH₂OCH₃ CF₃ CH₂CHCH₂CH₂CH₂CH₃ A-1656 CH₂OCH₂CH₂OCH₃ CF₃ CH₂CHCH₂ CH₂CH₂OCH₃ A-1657CH₂OCH₂CH₂OCH₃ CF₃ CH₂CCH CH₃ A-1658 CH₂OCH₂CH₂OCH₃ CF₃ CH₂CCH CH₂CH₃A-1659 CH₂OCH₂CH₂OCH₃ CF₃ CH₂CCH CH₂CH₂CH₃ A-1660 CH₂OCH₂CH₂OCH₃ CF₃CH₂CCH CH₂CH₂OCH₃ A-1661 CH₂OCH₂CH₂OCH₃ CF₃ CH₂C₆H₅ CH₃ A-1662CH₂OCH₂CH₂OCH₃ CF₃ CH₂C₆H₅ CH₂CH₃ A-1663 CH₂OCH₂CH₂OCH₃ CF₃ CH₂C₆H₅CH₂CH₂CH₃ A-1664 CH₂OCH₂CH₂OCH₃ CF₃ CH₂C₆H₅ CH₂CH₂OCH₃ A-1665CH₂OCH₂CH₂OCH₃ SO₂CH₃ CH₃ CH₃ A-1666 CH₂OCH₂CH₂OCH₃ SO₂CH₃ CH₃ CH₂CH₃A-1667 CH₂OCH₂CH₂OCH₃ SO₂CH₃ CH₃ CH₂CH₂CH₃ A-1668 CH₂OCH₂CH₂OCH₃ SO₂CH₃CH₃ CH₂CH₂OCH₃ A-1669 CH₂OCH₂CH₂OCH₃ SO₂CH₃ CH₂CH₃ CH₃ A-1670CH₂OCH₂CH₂OCH₃ SO₂CH₃ CH₂CH₃ CH₂CH₃ A-1671 CH₂OCH₂CH₂OCH₃ SO₂CH₃ CH₂CH₃CH₂CH₂CH₃ A-1672 CH₂OCH₂CH₂OCH₃ SO₂CH₃ CH₂CH₃ CH₂CH₂OCH₃ A-1673CH₂OCH₂CH₂OCH₃ SO₂CH₃ CH₂OCH₃ CH₃ A-1674 CH₂OCH₂CH₂OCH₃ SO₂CH₃ CH₂OCH₃CH₂CH₃ A-1675 CH₂OCH₂CH₂OCH₃ SO₂CH₃ CH₂OCH₃ CH₂CH₂CH₃ A-1676CH₂OCH₂CH₂OCH₃ SO₂CH₃ CH₂OCH₃ CH₂CH₂OCH₃ A-1677 CH₂OCH₂CH₂OCH₃ SO₂CH₃CH₂OCH₂CH₃ CH₃ A-1678 CH₂OCH₂CH₂OCH₃ SO₂CH₃ CH₂OCH₂CH₃ CH₂CH₃ A-1679CH₂OCH₂CH₂OCH₃ SO₂CH₃ CH₂OCH₂CH₃ CH₂CH₂CH₃ A-1680 CH₂OCH₂CH₂OCH₃ SO₂CH₃CH₂OCH₂CH₃ CH₂CH₂OCH₃ A-1681 CH₂OCH₂CH₂OCH₃ SO₂CH₃ CH₂(CO)OCH₃ CH₃A-1682 CH₂OCH₂CH₂OCH₃ SO₂CH₃ CH₂(CO)OCH₃ CH₂CH₃ A-1683 CH₂OCH₂CH₂OCH₃SO₂CH₃ CH₂(CO)OCH₃ CH₂CH₂CH₃ A-1684 CH₂OCH₂CH₂OCH₃ SO₂CH₃ CH₂(CO)OCH₃CH₂CH₂OCH₃ A-1685 CH₂OCH₂CH₂OCH₃ SO₂CH₃ CH₂CHCH₂ CH₃ A-1686CH₂OCH₂CH₂OCH₃ SO₂CH₃ CH₂CHCH₂ CH₂CH₃ A-1687 CH₂OCH₂CH₂OCH₃ SO₂CH₃CH₂CHCH₂ CH₂CH₂CH₃ A-1688 CH₂OCH₂CH₂OCH₃ SO₂CH₃ CH₂CHCH₂ CH₂CH₂OCH₃A-1689 CH₂OCH₂CH₂OCH₃ SO₂CH₃ CH₂CCH CH₃ A-1690 CH₂OCH₂CH₂OCH₃ SO₂CH₃CH₂CCH CH₂CH₃ A-1691 CH₂OCH₂CH₂OCH₃ SO₂CH₃ CH₂CCH CH₂CH₂CH₃ A-1692CH₂OCH₂CH₂OCH₃ SO₂CH₃ CH₂CCH CH₂CH₂OCH₃ A-1693 CH₂OCH₂CH₂OCH₃ SO₂CH₃CH₂C₆H₅ CH₃ A-1694 CH₂OCH₂CH₂OCH₃ SO₂CH₃ CH₂C₆H₅ CH₂CH₃ A-1695CH₂OCH₂CH₂OCH₃ SO₂CH₃ CH₂C₆H₅ CH₂CH₂CH₃ A-1696 CH₂OCH₂CH₂OCH₃ SO₂CH₃CH₂C₆H₅ CH₂CH₂OCH₃ A-1697 CH₂OCH₂CH₂OCH₃ NO₂ CH₃ CH₃ A-1698CH₂OCH₂CH₂OCH₃ NO₂ CH₃ CH₂CH₃ A-1699 CH₂OCH₂CH₂OCH₃ NO₂ CH₃ CH₂CH₂CH₃A-1700 CH₂OCH₂CH₂OCH₃ NO₂ CH₃ CH₂CH₂OCH₃ A-1701 CH₂OCH₂CH₂OCH₃ NO₂CH₂CH₃ CH₃ A-1702 CH₂OCH₂CH₂OCH₃ NO₂ CH₂CH₃ CH₂CH₃ A-1703 CH₂OCH₂CH₂OCH₃NO₂ CH₂CH₃ CH₂CH₂CH₃ A-1704 CH₂OCH₂CH₂OCH₃ NO₂ CH₂CH₃ CH₂CH₂OCH₃ A-1705CH₂OCH₂CH₂OCH₃ NO₂ CH₂OCH₃ CH₃ A-1706 CH₂OCH₂CH₂OCH₃ NO₂ CH₂OCH₃ CH₂CH₃A-1707 CH₂OCH₂CH₂OCH₃ NO₂ CH₂OCH₃ CH₂CH₂CH₃ A-1708 CH₂OCH₂CH₂OCH₃ NO₂CH₂OCH₃ CH₂CH₂OCH₃ A-1709 CH₂OCH₂CH₂OCH₃ NO₂ CH₂OCH₂CH₃ CH₃ A-1710CH₂OCH₂CH₂OCH₃ NO₂ CH₂OCH₂CH₃ CH₂CH₃ A-1711 CH₂OCH₂CH₂OCH₃ NO₂CH₂OCH₂CH₃ CH₂CH₂CH₃ A-1712 CH₂OCH₂CH₂OCH₃ NO₂ CH₂OCH₂CH₃ CH₂CH₂OCH₃A-1713 CH₂OCH₂CH₂OCH₃ NO₂ CH₂(CO)OCH₃ CH₃ A-1714 CH₂OCH₂CH₂OCH₃ NO₂CH₂(CO)OCH₃ CH₂CH₃ A-1715 CH₂OCH₂CH₂OCH₃ NO₂ CH₂(CO)OCH₃ CH₂CH₂CH₃A-1716 CH₂OCH₂CH₂OCH₃ NO₂ CH₂(CO)OCH₃ CH₂CH₂OCH₃ A-1717 CH₂OCH₂CH₂OCH₃NO₂ CH₂CHCH₂ CH₃ A-1718 CH₂OCH₂CH₂OCH₃ NO₂ CH₂CHCH₂ CH₂CH₃ A-1719CH₂OCH₂CH₂OCH₃ NO₂ CH₂CHCH₂ CH₂CH₂CH₃ A-1720 CH₂OCH₂CH₂OCH₃ NO₂ CH₂CHCH₂CH₂CH₂OCH₃ A-1721 CH₂OCH₂CH₂OCH₃ NO₂ CH₂CCH CH₃ A-1722 CH₂OCH₂CH₂OCH₃NO₂ CH₂CCH CH₂CH₃ A-1723 CH₂OCH₂CH₂OCH₃ NO₂ CH₂CCH CH₂CH₂CH₃ A-1724CH₂OCH₂CH₂OCH₃ NO₂ CH₂CCH CH₂CH₂OCH₃ A-1725 CH₂OCH₂CH₂OCH₃ NO₂ CH₂C₆H₅CH₃ A-1726 CH₂OCH₂CH₂OCH₃ NO₂ CH₂C₆H₅ CH₂CH₃ A-1727 CH₂OCH₂CH₂OCH₃ NO₂CH₂C₆H₅ CH₂CH₂CH₃ A-1728 CH₂OCH₂CH₂OCH₃ NO₂ CH₂C₆H₅ CH₂CH₂OCH₃ A-1729SO₂CH₃ H CH₃ CH₃ A-1730 SO₂CH₃ H CH₃ CH₂CH₃ A-1731 SO₂CH₃ H CH₃CH₂CH₂CH₃ A-1732 SO₂CH₃ H CH₃ CH₂CH₂OCH₃ A-1733 SO₂CH₃ H CH₂CH₃ CH₃A-1734 SO₂CH₃ H CH₂CH₃ CH₂CH₃ A-1735 SO₂CH₃ H CH₂CH₃ CH₂CH₂CH₃ A-1736SO₂CH₃ H CH₂CH₃ CH₂CH₂OCH₃ A-1737 SO₂CH₃ H CH₂OCH₃ CH₃ A-1738 SO₂CH₃ HCH₂OCH₃ CH₂CH₃ A-1739 SO₂CH₃ H CH₂OCH₃ CH₂CH₂CH₃ A-1740 SO₂CH₃ H CH₂OCH₃CH₂CH₂OCH₃ A-1741 SO₂CH₃ H CH₂OCH₂CH₃ CH₃ A-1742 SO₂CH₃ H CH₂OCH₂CH₃CH₂CH₃ A-1743 SO₂CH₃ H CH₂OCH₂CH₃ CH₂CH₂CH₃ A-1744 SO₂CH₃ H CH₂OCH₂CH₃CH₂CH₂OCH₃ A-1745 SO₂CH₃ H CH₂(CO)OCH₃ CH₃ A-1746 SO₂CH₃ H CH₂(CO)OCH₃CH₂CH₃ A-1747 SO₂CH₃ H CH₂(CO)OCH₃ CH₂CH₂CH₃ A-1748 SO₂CH₃ H CH₂(CO)OCH₃CH₂CH₂OCH₃ A-1749 SO₂CH₃ H CH₂CHCH₂ CH₃ A-1750 SO₂CH₃ H CH₂CHCH₂ CH₂CH₃A-1751 SO₂CH₃ H CH₂CHCH₂ CH₂CH₂CH₃ A-1752 SO₂CH₃ H CH₂CHCH₂ CH₂CH₂OCH₃A-1753 SO₂CH₃ H CH₂CCH CH₃ A-1754 SO₂CH₃ H CH₂CCH CH₂CH₃ A-1755 SO₂CH₃ HCH₂CCH CH₂CH₂CH₃ A-1756 SO₂CH₃ H CH₂CCH CH₂CH₂OCH₃ A-1757 SO₂CH₃ HCH₂C₆H₅ CH₃ A-1758 SO₂CH₃ H CH₂C₆H₅ CH₂CH₃ A-1759 SO₂CH₃ H CH₂C₆H₅CH₂CH₂CH₃ A-1760 SO₂CH₃ H CH₂C₆H₅ CH₂CH₂OCH₃ A-1761 SO₂CH₃ F CH₃ CH₃A-1762 SO₂CH₃ F CH₃ CH₂CH₃ A-1763 SO₂CH₃ F CH₃ CH₂CH₂CH₃ A-1764 SO₂CH₃ FCH₃ CH₂CH₂OCH₃ A-1765 SO₂CH₃ F CH₂CH₃ CH₃ A-1766 SO₂CH₃ F CH₂CH₃ CH₂CH₃A-1767 SO₂CH₃ F CH₂CH₃ CH₂CH₂CH₃ A-1768 SO₂CH₃ F CH₂CH₃ CH₂CH₂OCH₃A-1769 SO₂CH₃ F CH₂OCH₃ CH₃ A-1770 SO₂CH₃ F CH₂OCH₃ CH₂CH₃ A-1771 SO₂CH₃F CH₂OCH₃ CH₂CH₂CH₃ A-1772 SO₂CH₃ F CH₂OCH₃ CH₂CH₂OCH₃ A-1773 SO₂CH₃ FCH₂OCH₂CH₃ CH₃ A-1774 SO₂CH₃ F CH₂OCH₂CH₃ CH₂CH₃ A-1775 SO₂CH₃ FCH₂OCH₂CH₃ CH₂CH₂CH₃ A-1776 SO₂CH₃ F CH₂OCH₂CH₃ CH₂CH₂OCH₃ A-1777 SO₂CH₃F CH₂(CO)OCH₃ CH₃ A-1778 SO₂CH₃ F CH₂(CO)OCH₃ CH₂CH₃ A-1779 SO₂CH₃ FCH₂(CO)OCH₃ CH₂CH₂CH₃ A-1780 SO₂CH₃ F CH₂(CO)OCH₃ CH₂CH₂OCH₃ A-1781SO₂CH₃ F CH₂CHCH₂ CH₃ A-1782 SO₂CH₃ F CH₂CHCH₂ CH₂CH₃ A-1783 SO₂CH₃ FCH₂CHCH₂ CH₂CH₂CH₃ A-1784 SO₂CH₃ F CH₂CHCH₂ CH₂CH₂OCH₃ A-1785 SO₂CH₃ FCH₂CCH CH₃ A-1786 SO₂CH₃ F CH₂CCH CH₂CH₃ A-1787 SO₂CH₃ F CH₂CCHCH₂CH₂CH₃ A-1788 SO₂CH₃ F CH₂CCH CH₂CH₂OCH₃ A-1789 SO₂CH₃ F CH₂C₆H₅ CH₃A-1790 SO₂CH₃ F CH₂C₆H₅ CH₂CH₃ A-1791 SO₂CH₃ F CH₂C₆H₅ CH₂CH₂CH₃ A-1792SO₂CH₃ F CH₂C₆H₅ CH₂CH₂OCH₃ A-1793 SO₂CH₃ Cl CH₃ CH₃ A-1794 SO₂CH₃ ClCH₃ CH₂CH₃ A-1795 SO₂CH₃ Cl CH₃ CH₂CH₂CH₃ A-1796 SO₂CH₃ Cl CH₃CH₂CH₂OCH₃ A-1797 SO₂CH₃ Cl CH₂CH₃ CH₃ A-1798 SO₂CH₃ Cl CH₂CH₃ CH₂CH₃A-1799 SO₂CH₃ Cl CH₂CH₃ CH₂CH₂CH₃ A-1800 SO₂CH₃ Cl CH₂CH₃ CH₂CH₂OCH₃A-1801 SO₂CH₃ Cl CH₂OCH₃ CH₃ A-1802 SO₂CH₃ Cl CH₂OCH₃ CH₂CH₃ A-1803SO₂CH₃ Cl CH₂OCH₃ CH₂CH₂CH₃ A-1804 SO₂CH₃ Cl CH₂OCH₃ CH₂CH₂OCH₃ A-1805SO₂CH₃ Cl CH₂OCH₂CH₃ CH₃ A-1806 SO₂CH₃ Cl CH₂OCH₂CH₃ CH₂CH₃ A-1807SO₂CH₃ Cl CH₂OCH₂CH₃ CH₂CH₂CH₃ A-1808 SO₂CH₃ Cl CH₂OCH₂CH₃ CH₂CH₂OCH₃A-1809 SO₂CH₃ Cl CH₂(CO)OCH₃ CH₃ A-1810 SO₂CH₃ Cl CH₂(CO)OCH₃ CH₂CH₃A-1811 SO₂CH₃ Cl CH₂(CO)OCH₃ CH₂CH₂CH₃ A-1812 SO₂CH₃ Cl CH₂(CO)OCH₃CH₂CH₂OCH₃ A-1813 SO₂CH₃ Cl CH₂CHCH₂ CH₃ A-1814 SO₂CH₃ Cl CH₂CHCH₂CH₂CH₃ A-1815 SO₂CH₃ Cl CH₂CHCH₂ CH₂CH₂CH₃ A-1816 SO₂CH₃ Cl CH₂CHCH₂CH₂CH₂OCH₃ A-1817 SO₂CH₃ Cl CH₂CCH CH₃ A-1818 SO₂CH₃ Cl CH₂CCH CH₂CH₃A-1819 SO₂CH₃ Cl CH₂CCH CH₂CH₂CH₃ A-1820 SO₂CH₃ Cl CH₂CCH CH₂CH₂OCH₃A-1821 SO₂CH₃ Cl CH₂C₆H₅ CH₃ A-1822 SO₂CH₃ Cl CH₂C₆H₅ CH₂CH₃ A-1823SO₂CH₃ Cl CH₂C₆H₅ CH₂CH₂CH₃ A-1824 SO₂CH₃ Cl CH₂C₆H₅ CH₂CH₂OCH₃ A-1825SO₂CH₃ Br CH₃ CH₃ A-1826 SO₂CH₃ Br CH₃ CH₂CH₃ A-1827 SO₂CH₃ Br CH₃CH₂CH₂CH₃ A-1828 SO₂CH₃ Br CH₃ CH₂CH₂OCH₃ A-1829 SO₂CH₃ Br CH₂CH₃ CH₃A-1830 SO₂CH₃ Br CH₂CH₃ CH₂CH₃ A-1831 SO₂CH₃ Br CH₂CH₃ CH₂CH₂CH₃ A-1832SO₂CH₃ Br CH₂CH₃ CH₂CH₂OCH₃ A-1833 SO₂CH₃ Br CH₂OCH₃ CH₃ A-1834 SO₂CH₃Br CH₂OCH₃ CH₂CH₃ A-1835 SO₂CH₃ Br CH₂OCH₃ CH₂CH₂CH₃ A-1836 SO₂CH₃ BrCH₂OCH₃ CH₂CH₂OCH₃ A-1837 SO₂CH₃ Br CH₂OCH₂CH₃ CH₃ A-1838 SO₂CH₃ BrCH₂OCH₂CH₃ CH₂CH₃ A-1839 SO₂CH₃ Br CH₂OCH₂CH₃ CH₂CH₂CH₃ A-1840 SO₂CH₃ BrCH₂OCH₂CH₃ CH₂CH₂OCH₃ A-1841 SO₂CH₃ Br CH₂(CO)OCH₃ CH₃ A-1842 SO₂CH₃ BrCH₂(CO)OCH₃ CH₂CH₃ A-1843 SO₂CH₃ Br CH₂(CO)OCH₃ CH₂CH₂CH₃ A-1844 SO₂CH₃Br CH₂(CO)OCH₃ CH₂CH₂OCH₃ A-1845 SO₂CH₃ Br CH₂CHCH₂ CH₃ A-1846 SO₂CH₃ BrCH₂CHCH₂ CH₂CH₃ A-1847 SO₂CH₃ Br CH₂CHCH₂ CH₂CH₂CH₃ A-1848 SO₂CH₃ BrCH₂CHCH₂ CH₂CH₂OCH₃ A-1849 SO₂CH₃ Br CH₂CCH CH₃ A-1850 SO₂CH₃ Br CH₂CCHCH₂CH₃ A-1851 SO₂CH₃ Br CH₂CCH CH₂CH₂CH₃ A-1852 SO₂CH₃ Br CH₂CCHCH₂CH₂OCH₃ A-1853 SO₂CH₃ Br CH₂C₆H₅ CH₃ A-1854 SO₂CH₃ Br CH₂C₆H₅ CH₂CH₃A-1855 SO₂CH₃ Br CH₂C₆H₅ CH₂CH₂CH₃ A-1856 SO₂CH₃ Br CH₂C₆H₅ CH₂CH₂OCH₃A-1857 SO₂CH₃ CN CH₃ CH₃ A-1858 SO₂CH₃ CN CH₃ CH₂CH₃ A-1859 SO₂CH₃ CNCH₃ CH₂CH₂CH₃ A-1860 SO₂CH₃ CN CH₃ CH₂CH₂OCH₃ A-1861 SO₂CH₃ CN CH₂CH₃CH₃ A-1862 SO₂CH₃ CN CH₂CH₃ CH₂CH₃ A-1863 SO₂CH₃ CN CH₂CH₃ CH₂CH₂CH₃A-1864 SO₂CH₃ CN CH₂CH₃ CH₂CH₂OCH₃ A-1865 SO₂CH₃ CN CH₂OCH₃ CH₃ A-1866SO₂CH₃ CN CH₂OCH₃ CH₂CH₃ A-1867 SO₂CH₃ CN CH₂OCH₃ CH₂CH₂CH₃ A-1868SO₂CH₃ CN CH₂OCH₃ CH₂CH₂OCH₃ A-1869 SO₂CH₃ CN CH₂OCH₂CH₃ CH₃ A-1870SO₂CH₃ CN CH₂OCH₂CH₃ CH₂CH₃ A-1871 SO₂CH₃ CN CH₂OCH₂CH₃ CH₂CH₂CH₃ A-1872SO₂CH₃ CN CH₂OCH₂CH₃ CH₂CH₂OCH₃ A-1873 SO₂CH₃ CN CH₂(CO)OCH₃ CH₃ A-1874SO₂CH₃ CN CH₂(CO)OCH₃ CH₂CH₃ A-1875 SO₂CH₃ CN CH₂(CO)OCH₃ CH₂CH₂CH₃A-1876 SO₂CH₃ CN CH₂(CO)OCH₃ CH₂CH₂OCH₃ A-1877 SO₂CH₃ CN CH₂CHCH₂ CH₃A-1878 SO₂CH₃ CN CH₂CHCH₂ CH₂CH₃ A-1879 SO₂CH₃ CN CH₂CHCH₂ CH₂CH₂CH₃A-1880 SO₂CH₃ CN CH₂CHCH₂ CH₂CH₂OCH₃ A-1881 SO₂CH₃ CN CH₂CCH CH₃ A-1882SO₂CH₃ CN CH₂CCH CH₂CH₃ A-1883 SO₂CH₃ CN CH₂CCH CH₂CH₂CH₃ A-1884 SO₂CH₃CN CH₂CCH CH₂CH₂OCH₃ A-1885 SO₂CH₃ CN CH₂C₆H₅ CH₃ A-1886 SO₂CH₃ CNCH₂C₆H₅ CH₂CH₃ A-1887 SO₂CH₃ CN CH₂C₆H₅ CH₂CH₂CH₃ A-1888 SO₂CH₃ CNCH₂C₆H₅ CH₂CH₂OCH₃ A-1889 SO₂CH₃ CH₃ CH₃ CH₃ A-1890 SO₂CH₃ CH₃ CH₃CH₂CH₃ A-1891 SO₂CH₃ CH₃ CH₃ CH₂CH₂CH₃ A-1892 SO₂CH₃ CH₃ CH₃ CH₂CH₂OCH₃A-1893 SO₂CH₃ CH₃ CH₂CH₃ CH₃ A-1894 SO₂CH₃ CH₃ CH₂CH₃ CH₂CH₃ A-1895SO₂CH₃ CH₃ CH₂CH₃ CH₂CH₂CH₃ A-1896 SO₂CH₃ CH₃ CH₂CH₃ CH₂CH₂OCH₃ A-1897SO₂CH₃ CH₃ CH₂OCH₃ CH₃ A-1898 SO₂CH₃ CH₃ CH₂OCH₃ CH₂CH₃ A-1899 SO₂CH₃CH₃ CH₂OCH₃ CH₂CH₂CH₃ A-1900 SO₂CH₃ CH₃ CH₂OCH₃ CH₂CH₂OCH₃ A-1901 SO₂CH₃CH₃ CH₂OCH₂CH₃ CH₃ A-1902 SO₂CH₃ CH₃ CH₂OCH₂CH₃ CH₂CH₃ A-1903 SO₂CH₃ CH₃CH₂OCH₂CH₃ CH₂CH₂CH₃ A-1904 SO₂CH₃ CH₃ CH₂OCH₂CH₃ CH₂CH₂OCH₃ A-1905SO₂CH₃ CH₃ CH₂(CO)OCH₃ CH₃ A-1906 SO₂CH₃ CH₃ CH₂(CO)OCH₃ CH₂CH₃ A-1907SO₂CH₃ CH₃ CH₂(CO)OCH₃ CH₂CH₂CH₃ A-1908 SO₂CH₃ CH₃ CH₂(CO)OCH₃CH₂CH₂OCH₃ A-1909 SO₂CH₃ CH₃ CH₂CHCH₂ CH₃ A-1910 SO₂CH₃ CH₃ CH₂CHCH₂CH₂CH₃ A-1911 SO₂CH₃ CH₃ CH₂CHCH₂ CH₂CH₂CH₃ A-1912 SO₂CH₃ CH₃ CH₂CHCH₂CH₂CH₂OCH₃ A-1913 SO₂CH₃ CH₃ CH₂CCH CH₃ A-1914 SO₂CH₃ CH₃ CH₂CCH CH₂CH₃A-1915 SO₂CH₃ CH₃ CH₂CCH CH₂CH₂CH₃ A-1916 SO₂CH₃ CH₃ CH₂CCH CH₂CH₂OCH₃A-1917 SO₂CH₃ CH₃ CH₂C₆H₅ CH₃ A-1918 SO₂CH₃ CH₃ CH₂C₆H₅ CH₂CH₃ A-1919SO₂CH₃ CH₃ CH₂C₆H₅ CH₂CH₂CH₃ A-1920 SO₂CH₃ CH₃ CH₂C₆H₅ CH₂CH₂OCH₃ A-1921SO₂CH₃ CF₃ CH₃ CH₃ A-1922 SO₂CH₃ CF₃ CH₃ CH₂CH₃ A-1923 SO₂CH₃ CF₃ CH₃CH₂CH₂CH₃ A-1924 SO₂CH₃ CF₃ CH₃ CH₂CH₂OCH₃ A-1925 SO₂CH₃ CF₃ CH₂CH₃ CH₃A-1926 SO₂CH₃ CF₃ CH₂CH₃ CH₂CH₃ A-1927 SO₂CH₃ CF₃ CH₂CH₃ CH₂CH₂CH₃A-1928 SO₂CH₃ CF₃ CH₂CH₃ CH₂CH₂OCH₃ A-1929 SO₂CH₃ CF₃ CH₂OCH₃ CH₃ A-1930SO₂CH₃ CF₃ CH₂OCH₃ CH₂CH₃ A-1931 SO₂CH₃ CF₃ CH₂OCH₃ CH₂CH₂CH₃ A-1932SO₂CH₃ CF₃ CH₂OCH₃ CH₂CH₂OCH₃ A-1933 SO₂CH₃ CF₃ CH₂OCH₂CH₃ CH₃ A-1934SO₂CH₃ CF₃ CH₂OCH₂CH₃ CH₂CH₃ A-1935 SO₂CH₃ CF₃ CH₂OCH₂CH₃ CH₂CH₂CH₃A-1936 SO₂CH₃ CF₃ CH₂OCH₂CH₃ CH₂CH₂OCH₃ A-1937 SO₂CH₃ CF₃ CH₂(CO)OCH₃CH₃ A-1938 SO₂CH₃ CF₃ CH₂(CO)OCH₃ CH₂CH₃ A-1939 SO₂CH₃ CF₃ CH₂(CO)OCH₃CH₂CH₂CH₃ A-1940 SO₂CH₃ CF₃ CH₂(CO)OCH₃ CH₂CH₂OCH₃ A-1941 SO₂CH₃ CF₃CH₂CHCH₂ CH₃ A-1942 SO₂CH₃ CF₃ CH₂CHCH₂ CH₂CH₃ A-1943 SO₂CH₃ CF₃CH₂CHCH₂ CH₂CH₂CH₃ A-1944 SO₂CH₃ CF₃ CH₂CHCH₂ CH₂CH₂OCH₃ A-1945 SO₂CH₃CF₃ CH₂CCH CH₃ A-1946 SO₂CH₃ CF₃ CH₂CCH CH₂CH₃ A-1947 SO₂CH₃ CF₃ CH₂CCHCH₂CH₂CH₃ A-1948 SO₂CH₃ CF₃ CH₂CCH CH₂CH₂OCH₃ A-1949 SO₂CH₃ CF₃ CH₂C₆H₅CH₃ A-1950 SO₂CH₃ CF₃ CH₂C₆H₅ CH₂CH₃ A-1951 SO₂CH₃ CF₃ CH₂C₆H₅ CH₂CH₂CH₃A-1952 SO₂CH₃ CF₃ CH₂C₆H₅ CH₂CH₂OCH₃ A-1953 SO₂CH₃ SO₂CH₃ CH₃ CH₃ A-1954SO₂CH₃ SO₂CH₃ CH₃ CH₂CH₃ A-1955 SO₂CH₃ SO₂CH₃ CH₃ CH₂CH₂CH₃ A-1956SO₂CH₃ SO₂CH₃ CH₃ CH₂CH₂OCH₃ A-1957 SO₂CH₃ SO₂CH₃ CH₂CH₃ CH₃ A-1958SO₂CH₃ SO₂CH₃ CH₂CH₃ CH₂CH₃ A-1959 SO₂CH₃ SO₂CH₃ CH₂CH₃ CH₂CH₂CH₃ A-1960SO₂CH₃ SO₂CH₃ CH₂CH₃ CH₂CH₂OCH₃ A-1961 SO₂CH₃ SO₂CH₃ CH₂OCH₃ CH₃ A-1962SO₂CH₃ SO₂CH₃ CH₂OCH₃ CH₂CH₃ A-1963 SO₂CH₃ SO₂CH₃ CH₂OCH₃ CH₂CH₂CH₃A-1964 SO₂CH₃ SO₂CH₃ CH₂OCH₃ CH₂CH₂OCH₃ A-1965 SO₂CH₃ SO₂CH₃ CH₂OCH₂CH₃CH₃ A-1966 SO₂CH₃ SO₂CH₃ CH₂OCH₂CH₃ CH₂CH₃ A-1967 SO₂CH₃ SO₂CH₃CH₂OCH₂CH₃ CH₂CH₂CH₃ A-1968 SO₂CH₃ SO₂CH₃ CH₂OCH₂CH₃ CH₂CH₂OCH₃ A-1969SO₂CH₃ SO₂CH₃ CH₂(CO)OCH₃ CH₃ A-1970 SO₂CH₃ SO₂CH₃ CH₂(CO)OCH₃ CH₂CH₃A-1971 SO₂CH₃ SO₂CH₃ CH₂(CO)OCH₃ CH₂CH₂CH₃ A-1972 SO₂CH₃ SO₂CH₃CH₂(CO)OCH₃ CH₂CH₂OCH₃ A-1973 SO₂CH₃ SO₂CH₃ CH₂CHCH₂ CH₃ A-1974 SO₂CH₃SO₂CH₃ CH₂CHCH₂ CH₂CH₃ A-1975 SO₂CH₃ SO₂CH₃ CH₂CHCH₂ CH₂CH₂CH₃ A-1976SO₂CH₃ SO₂CH₃ CH₂CHCH₂ CH₂CH₂OCH₃ A-1977 SO₂CH₃ SO₂CH₃ CH₂CCH CH₃ A-1978SO₂CH₃ SO₂CH₃ CH₂CCH CH₂CH₃ A-1979 SO₂CH₃ SO₂CH₃ CH₂CCH CH₂CH₂CH₃ A-1980SO₂CH₃ SO₂CH₃ CH₂CCH CH₂CH₂OCH₃ A-1981 SO₂CH₃ SO₂CH₃ CH₂C₆H₅ CH₃ A-1982SO₂CH₃ SO₂CH₃ CH₂C₆H₅ CH₂CH₃ A-1983 SO₂CH₃ SO₂CH₃ CH₂C₆H₅ CH₂CH₂CH₃A-1984 SO₂CH₃ SO₂CH₃ CH₂C₆H₅ CH₂CH₂OCH₃ A-1985 SO₂CH₃ NO₂ CH₃ CH₃ A-1986SO₂CH₃ NO₂ CH₃ CH₂CH₃ A-1987 SO₂CH₃ NO₂ CH₃ CH₂CH₂CH₃ A-1988 SO₂CH₃ NO₂CH₃ CH₂CH₂OCH₃ A-1989 SO₂CH₃ NO₂ CH₂CH₃ CH₃ A-1990 SO₂CH₃ NO₂ CH₂CH₃CH₂CH₃ A-1991 SO₂CH₃ NO₂ CH₂CH₃ CH₂CH₂CH₃ A-1992 SO₂CH₃ NO₂ CH₂CH₃CH₂CH₂OCH₃ A-1993 SO₂CH₃ NO₂ CH₂OCH₃ CH₃ A-1994 SO₂CH₃ NO₂ CH₂OCH₃CH₂CH₃ A-1995 SO₂CH₃ NO₂ CH₂OCH₃ CH₂CH₂CH₃ A-1996 SO₂CH₃ NO₂ CH₂OCH₃CH₂CH₂OCH₃ A-1997 SO₂CH₃ NO₂ CH₂OCH₂CH₃ CH₃ A-1998 SO₂CH₃ NO₂ CH₂OCH₂CH₃CH₂CH₃ A-1999 SO₂CH₃ NO₂ CH₂OCH₂CH₃ CH₂CH₂CH₃ A-2000 SO₂CH₃ NO₂CH₂OCH₂CH₃ CH₂CH₂OCH₃ A-2001 SO₂CH₃ NO₂ CH₂(CO)OCH₃ CH₃ A-2002 SO₂CH₃NO₂ CH₂(CO)OCH₃ CH₂CH₃ A-2003 SO₂CH₃ NO₂ CH₂(CO)OCH₃ CH₂CH₂CH₃ A-2004SO₂CH₃ NO₂ CH₂(CO)OCH₃ CH₂CH₂OCH₃ A-2005 SO₂CH₃ NO₂ CH₂CHCH₂ CH₃ A-2006SO₂CH₃ NO₂ CH₂CHCH₂ CH₂CH₃ A-2007 SO₂CH₃ NO₂ CH₂CHCH₂ CH₂CH₂CH₃ A-2008SO₂CH₃ NO₂ CH₂CHCH₂ CH₂CH₂OCH₃ A-2009 SO₂CH₃ NO₂ CH₂CCH CH₃ A-2010SO₂CH₃ NO₂ CH₂CCH CH₂CH₃ A-2011 SO₂CH₃ NO₂ CH₂CCH CH₂CH₂CH₃ A-2012SO₂CH₃ NO₂ CH₂CCH CH₂CH₂OCH₃ A-2013 SO₂CH₃ NO₂ CH₂C₆H₅ CH₃ A-2014 SO₂CH₃NO₂ CH₂C₆H₅ CH₂CH₃ A-2015 SO₂CH₃ NO₂ CH₂C₆H₅ CH₂CH₂CH₃ A-2016 SO₂CH₃ NO₂CH₂C₆H₅ CH₂CH₂OCH₃ A-2017 CF₃ H CH₃ CH₃ A-2018 CF₃ H CH₃ CH₂CH₃ A-2019CF₃ H CH₃ CH₂CH₂CH₃ A-2020 CF₃ H CH₃ CH₂CH₂OCH₃ A-2021 CF₃ H CH₂CH₃ CH₃A-2022 CF₃ H CH₂CH₃ CH₂CH₃ A-2023 CF₃ H CH₂CH₃ CH₂CH₂CH₃ A-2024 CF₃ HCH₂CH₃ CH₂CH₂OCH₃ A-2025 CF₃ H CH₂OCH₃ CH₃ A-2026 CF₃ H CH₂OCH₃ CH₂CH₃A-2027 CF₃ H CH₂OCH₃ CH₂CH₂CH₃ A-2028 CF₃ H CH₂OCH₃ CH₂CH₂OCH₃ A-2029CF₃ H CH₂OCH₂CH₃ CH₃ A-2030 CF₃ H CH₂OCH₂CH₃ CH₂CH₃ A-2031 CF₃ HCH₂OCH₂CH₃ CH₂CH₂CH₃ A-2032 CF₃ H CH₂OCH₂CH₃ CH₂CH₂OCH₃ A-2033 CF₃ HCH₂(CO)OCH₃ CH₃ A-2034 CF₃ H CH₂(CO)OCH₃ CH₂CH₃ A-2035 CF₃ H CH₂(CO)OCH₃CH₂CH₂CH₃ A-2036 CF₃ H CH₂(CO)OCH₃ CH₂CH₂OCH₃ A-2037 CF₃ H CH₂CHCH₂ CH₃A-2038 CF₃ H CH₂CHCH₂ CH₂CH₃ A-2039 CF₃ H CH₂CHCH₂ CH₂CH₂CH₃ A-2040 CF₃H CH₂CHCH₂ CH₂CH₂OCH₃ A-2041 CF₃ H CH₂CCH CH₃ A-2042 CF₃ H CH₂CCH CH₂CH₃A-2043 CF₃ H CH₂CCH CH₂CH₂CH₃ A-2044 CF₃ H CH₂CCH CH₂CH₂OCH₃ A-2045 CF₃H CH₂C₆H₅ CH₃ A-2046 CF₃ H CH₂C₆H₅ CH₂CH₃ A-2047 CF₃ H CH₂C₆H₅ CH₂CH₂CH₃A-2048 CF₃ H CH₂C₆H₅ CH₂CH₂OCH₃ A-2049 CF₃ F CH₃ CH₃ A-2050 CF₃ F CH₃CH₂CH₃ A-2051 CF₃ F CH₃ CH₂CH₂CH₃ A-2052 CF₃ F CH₃ CH₂CH₂OCH₃ A-2053 CF₃F CH₂CH₃ CH₃ A-2054 CF₃ F CH₂CH₃ CH₂CH₃ A-2055 CF₃ F CH₂CH₃ CH₂CH₂CH₃A-2056 CF₃ F CH₂CH₃ CH₂CH₂OCH₃ A-2057 CF₃ F CH₂OCH₃ CH₃ A-2058 CF₃ FCH₂OCH₃ CH₂CH₃ A-2059 CF₃ F CH₂OCH₃ CH₂CH₂CH₃ A-2060 CF₃ F CH₂OCH₃CH₂CH₂OCH₃ A-2061 CF₃ F CH₂OCH₂CH₃ CH₃ A-2062 CF₃ F CH₂OCH₂CH₃ CH₂CH₃A-2063 CF₃ F CH₂OCH₂CH₃ CH₂CH₂CH₃ A-2064 CF₃ F CH₂OCH₂CH₃ CH₂CH₂OCH₃A-2065 CF₃ F CH₂(CO)OCH₃ CH₃ A-2066 CF₃ F CH₂(CO)OCH₃ CH₂CH₃ A-2067 CF₃F CH₂(CO)OCH₃ CH₂CH₂CH₃ A-2068 CF₃ F CH₂(CO)OCH₃ CH₂CH₂OCH₃ A-2069 CF₃ FCH₂CHCH₂ CH₃ A-2070 CF₃ F CH₂CHCH₂ CH₂CH₃ A-2071 CF₃ F CH₂CHCH₂CH₂CH₂CH₃ A-2072 CF₃ F CH₂CHCH₂ CH₂CH₂OCH₃ A-2073 CF₃ F CH₂CCH CH₃A-2074 CF₃ F CH₂CCH CH₂CH₃ A-2075 CF₃ F CH₂CCH CH₂CH₂CH₃ A-2076 CF₃ FCH₂CCH CH₂CH₂OCH₃ A-2077 CF₃ F CH₂C₆H₅ CH₃ A-2078 CF₃ F CH₂C₆H₅ CH₂CH₃A-2079 CF₃ F CH₂C₆H₅ CH₂CH₂CH₃ A-2080 CF₃ F CH₂C₆H₅ CH₂CH₂OCH₃ A-2081CF₃ Cl CH₃ CH₃ A-2082 CF₃ Cl CH₃ CH₂CH₃ A-2083 CF₃ Cl CH₃ CH₂CH₂CH₃A-2084 CF₃ Cl CH₃ CH₂CH₂OCH₃ A-2085 CF₃ Cl CH₂CH₃ CH₃ A-2086 CF₃ ClCH₂CH₃ CH₂CH₃ A-2087 CF₃ Cl CH₂CH₃ CH₂CH₂CH₃ A-2088 CF₃ Cl CH₂CH₃CH₂CH₂OCH₃ A-2089 CF₃ Cl CH₂OCH₃ CH₃ A-2090 CF₃ Cl CH₂OCH₃ CH₂CH₃ A-2091CF₃ Cl CH₂OCH₃ CH₂CH₂CH₃ A-2092 CF₃ Cl CH₂OCH₃ CH₂CH₂OCH₃ A-2093 CF₃ ClCH₂OCH₂CH₃ CH₃ A-2094 CF₃ Cl CH₂OCH₂CH₃ CH₂CH₃ A-2095 CF₃ Cl CH₂OCH₂CH₃CH₂CH₂CH₃ A-2096 CF₃ Cl CH₂OCH₂CH₃ CH₂CH₂OCH₃ A-2097 CF₃ Cl CH₂(CO)OCH₃CH₃ A-2098 CF₃ Cl CH₂(CO)OCH₃ CH₂CH₃ A-2099 CF₃ Cl CH₂(CO)OCH₃ CH₂CH₂CH₃A-2100 CF₃ Cl CH₂(CO)OCH₃ CH₂CH₂OCH₃ A-2101 CF₃ Cl CH₂CHCH₂ CH₃ A-2102CF₃ Cl CH₂CHCH₂ CH₂CH₃ A-2103 CF₃ Cl CH₂CHCH₂ CH₂CH₂CH₃ A-2104 CF₃ ClCH₂CHCH₂ CH₂CH₂OCH₃ A-2105 CF₃ Cl CH₂CCH CH₃ A-2106 CF₃ Cl CH₂CCH CH₂CH₃A-2107 CF₃ Cl CH₂CCH CH₂CH₂CH₃ A-2108 CF₃ Cl CH₂CCH CH₂CH₂OCH₃ A-2109CF₃ Cl CH₂C₆H₅ CH₃ A-2110 CF₃ Cl CH₂C₆H₅ CH₂CH₃ A-2111 CF₃ Cl CH₂C₆H₅CH₂CH₂CH₃ A-2112 CF₃ Cl CH₂C₆H₅ CH₂CH₂OCH₃ A-2113 CF₃ Br CH₃ CH₃ A-2114CF₃ Br CH₃ CH₂CH₃ A-2115 CF₃ Br CH₃ CH₂CH₂CH₃ A-2116 CF₃ Br CH₃CH₂CH₂OCH₃ A-2117 CF₃ Br CH₂CH₃ CH₃ A-2118 CF₃ Br CH₂CH₃ CH₂CH₃ A-2119CF₃ Br CH₂CH₃ CH₂CH₂CH₃ A-2120 CF₃ Br CH₂CH₃ CH₂CH₂OCH₃ A-2121 CF₃ BrCH₂OCH₃ CH₃ A-2122 CF₃ Br CH₂OCH₃ CH₂CH₃ A-2123 CF₃ Br CH₂OCH₃ CH₂CH₂CH₃A-2124 CF₃ Br CH₂OCH₃ CH₂CH₂OCH₃ A-2125 CF₃ Br CH₂OCH₂CH₃ CH₃ A-2126 CF₃Br CH₂OCH₂CH₃ CH₂CH₃ A-2127 CF₃ Br CH₂OCH₂CH₃ CH₂CH₂CH₃ A-2128 CF₃ BrCH₂OCH₂CH₃ CH₂CH₂OCH₃ A-2129 CF₃ Br CH₂(CO)OCH₃ CH₃ A-2130 CF₃ BrCH₂(CO)OCH₃ CH₂CH₃ A-2131 CF₃ Br CH₂(CO)OCH₃ CH₂CH₂CH₃ A-2132 CF₃ BrCH₂(CO)OCH₃ CH₂CH₂OCH₃ A-2133 CF₃ Br CH₂CHCH₂ CH₃ A-2134 CF₃ Br CH₂CHCH₂CH₂CH₃ A-2135 CF₃ Br CH₂CHCH₂ CH₂CH₂CH₃ A-2136 CF₃ Br CH₂CHCH₂CH₂CH₂OCH₃ A-2137 CF₃ Br CH₂CCH CH₃ A-2138 CF₃ Br CH₂CCH CH₂CH₃ A-2139CF₃ Br CH₂CCH CH₂CH₂CH₃ A-2140 CF₃ Br CH₂CCH CH₂CH₂OCH₃ A-2141 CF₃ BrCH₂C₆H₅ CH₃ A-2142 CF₃ Br CH₂C₆H₅ CH₂CH₃ A-2143 CF₃ Br CH₂C₆H₅ CH₂CH₂CH₃A-2144 CF₃ Br CH₂C₆H₅ CH₂CH₂OCH₃ A-2145 CF₃ CN CH₃ CH₃ A-2146 CF₃ CN CH₃CH₂CH₃ A-2147 CF₃ CN CH₃ CH₂CH₂CH₃ A-2148 CF₃ CN CH₃ CH₂CH₂OCH₃ A-2149CF₃ CN CH₂CH₃ CH₃ A-2150 CF₃ CN CH₂CH₃ CH₂CH₃ A-2151 CF₃ CN CH₂CH₃CH₂CH₂CH₃ A-2152 CF₃ CN CH₂CH₃ CH₂CH₂OCH₃ A-2153 CF₃ CN CH₂OCH₃ CH₃A-2154 CF₃ CN CH₂OCH₃ CH₂CH₃ A-2155 CF₃ CN CH₂OCH₃ CH₂CH₂CH₃ A-2156 CF₃CN CH₂OCH₃ CH₂CH₂OCH₃ A-2157 CF₃ CN CH₂OCH₂CH₃ CH₃ A-2158 CF₃ CNCH₂OCH₂CH₃ CH₂CH₃ A-2159 CF₃ CN CH₂OCH₂CH₃ CH₂CH₂CH₃ A-2160 CF₃ CNCH₂OCH₂CH₃ CH₂CH₂OCH₃ A-2161 CF₃ CN CH₂(CO)OCH₃ CH₃ A-2162 CF₃ CNCH₂(CO)OCH₃ CH₂CH₃ A-2163 CF₃ CN CH₂(CO)OCH₃ CH₂CH₂CH₃ A-2164 CF₃ CNCH₂(CO)OCH₃ CH₂CH₂OCH₃ A-2165 CF₃ CN CH₂CHCH₂ CH₃ A-2166 CF₃ CN CH₂CHCH₂CH₂CH₃ A-2167 CF₃ CN CH₂CHCH₂ CH₂CH₂CH₃ A-2168 CF₃ CN CH₂CHCH₂CH₂CH₂OCH₃ A-2169 CF₃ CN CH₂CCH CH₃ A-2170 CF₃ CN CH₂CCH CH₂CH₃ A-2171CF₃ CN CH₂CCH CH₂CH₂CH₃ A-2172 CF₃ CN CH₂CCH CH₂CH₂OCH₃ A-2173 CF₃ CNCH₂C₆H₅ CH₃ A-2174 CF₃ CN CH₂C₆H₅ CH₂CH₃ A-2175 CF₃ CN CH₂C₆H₅ CH₂CH₂CH₃A-2176 CF₃ CN CH₂C₆H₅ CH₂CH₂OCH₃ A-2177 CF₃ CH₃ CH₃ CH₃ A-2178 CF₃ CH₃CH₃ CH₂CH₃ A-2179 CF₃ CH₃ CH₃ CH₂CH₂CH₃ A-2180 CF₃ CH₃ CH₃ CH₂CH₂OCH₃A-2181 CF₃ CH₃ CH₂CH₃ CH₃ A-2182 CF₃ CH₃ CH₂CH₃ CH₂CH₃ A-2183 CF₃ CH₃CH₂CH₃ CH₂CH₂CH₃ A-2184 CF₃ CH₃ CH₂CH₃ CH₂CH₂OCH₃ A-2185 CF₃ CH₃ CH₂OCH₃CH₃ A-2186 CF₃ CH₃ CH₂OCH₃ CH₂CH₃ A-2187 CF₃ CH₃ CH₂OCH₃ CH₂CH₂CH₃A-2188 CF₃ CH₃ CH₂OCH₃ CH₂CH₂OCH₃ A-2189 CF₃ CH₃ CH₂OCH₂CH₃ CH₃ A-2190CF₃ CH₃ CH₂OCH₂CH₃ CH₂CH₃ A-2191 CF₃ CH₃ CH₂OCH₂CH₃ CH₂CH₂CH₃ A-2192 CF₃CH₃ CH₂OCH₂CH₃ CH₂CH₂OCH₃ A-2193 CF₃ CH₃ CH₂(CO)OCH₃ CH₃ A-2194 CF₃ CH₃CH₂(CO)OCH₃ CH₂CH₃ A-2195 CF₃ CH₃ CH₂(CO)OCH₃ CH₂CH₂CH₃ A-2196 CF₃ CH₃CH₂(CO)OCH₃ CH₂CH₂OCH₃ A-2197 CF₃ CH₃ CH₂CHCH₂ CH₃ A-2198 CF₃ CH₃CH₂CHCH₂ CH₂CH₃ A-2199 CF₃ CH₃ CH₂CHCH₂ CH₂CH₂CH₃ A-2200 CF₃ CH₃CH₂CHCH₂ CH₂CH₂OCH₃ A-2201 CF₃ CH₃ CH₂CCH CH₃ A-2202 CF₃ CH₃ CH₂CCHCH₂CH₃ A-2203 CF₃ CH₃ CH₂CCH CH₂CH₂CH₃ A-2204 CF₃ CH₃ CH₂CCH CH₂CH₂OCH₃A-2205 CF₃ CH₃ CH₂C₆H₅ CH₃ A-2206 CF₃ CH₃ CH₂C₆H₅ CH₂CH₃ A-2207 CF₃ CH₃CH₂C₆H₅ CH₂CH₂CH₃ A-2208 CF₃ CH₃ CH₂C₆H₅ CH₂CH₂OCH₃ A-2209 CF₃ CF₃ CH₃CH₃ A-2210 CF₃ CF₃ CH₃ CH₂CH₃ A-2211 CF₃ CF₃ CH₃ CH₂CH₂CH₃ A-2212 CF₃CF₃ CH₃ CH₂CH₂OCH₃ A-2213 CF₃ CF₃ CH₂CH₃ CH₃ A-2214 CF₃ CF₃ CH₂CH₃CH₂CH₃ A-2215 CF₃ CF₃ CH₂CH₃ CH₂CH₂CH₃ A-2216 CF₃ CF₃ CH₂CH₃ CH₂CH₂OCH₃A-2217 CF₃ CF₃ CH₂OCH₃ CH₃ A-2218 CF₃ CF₃ CH₂OCH₃ CH₂CH₃ A-2219 CF₃ CF₃CH₂OCH₃ CH₂CH₂CH₃ A-2220 CF₃ CF₃ CH₂OCH₃ CH₂CH₂OCH₃ A-2221 CF₃ CF₃CH₂OCH₂CH₃ CH₃ A-2222 CF₃ CF₃ CH₂OCH₂CH₃ CH₂CH₃ A-2223 CF₃ CF₃CH₂OCH₂CH₃ CH₂CH₂CH₃ A-2224 CF₃ CF₃ CH₂OCH₂CH₃ CH₂CH₂OCH₃ A-2225 CF₃ CF₃CH₂(CO)OCH₃ CH₃ A-2226 CF₃ CF₃ CH₂(CO)OCH₃ CH₂CH₃ A-2227 CF₃ CF₃CH₂(CO)OCH₃ CH₂CH₂CH₃ A-2228 CF₃ CF₃ CH₂(CO)OCH₃ CH₂CH₂OCH₃ A-2229 CF₃CF₃ CH₂CHCH₂ CH₃ A-2230 CF₃ CF₃ CH₂CHCH₂ CH₂CH₃ A-2231 CF₃ CF₃ CH₂CHCH₂CH₂CH₂CH₃ A-2232 CF₃ CF₃ CH₂CHCH₂ CH₂CH₂OCH₃ A-2233 CF₃ CF₃ CH₂CCH CH₃A-2234 CF₃ CF₃ CH₂CCH CH₂CH₃ A-2235 CF₃ CF₃ CH₂CCH CH₂CH₂CH₃ A-2236 CF₃CF₃ CH₂CCH CH₂CH₂OCH₃ A-2237 CF₃ CF₃ CH₂C₆H₅ CH₃ A-2238 CF₃ CF₃ CH₂C₆H₅CH₂CH₃ A-2239 CF₃ CF₃ CH₂C₆H₅ CH₂CH₂CH₃ A-2240 CF₃ CF₃ CH₂C₆H₅CH₂CH₂OCH₃ A-2241 CF₃ SO₂CH₃ CH₃ CH₃ A-2242 CF₃ SO₂CH₃ CH₃ CH₂CH₃ A-2243CF₃ SO₂CH₃ CH₃ CH₂CH₂CH₃ A-2244 CF₃ SO₂CH₃ CH₃ CH₂CH₂OCH₃ A-2245 CF₃SO₂CH₃ CH₂CH₃ CH₃ A-2246 CF₃ SO₂CH₃ CH₂CH₃ CH₂CH₃ A-2247 CF₃ SO₂CH₃CH₂CH₃ CH₂CH₂CH₃ A-2248 CF₃ SO₂CH₃ CH₂CH₃ CH₂CH₂OCH₃ A-2249 CF₃ SO₂CH₃CH₂OCH₃ CH₃ A-2250 CF₃ SO₂CH₃ CH₂OCH₃ CH₂CH₃ A-2251 CF₃ SO₂CH₃ CH₂OCH₃CH₂CH₂CH₃ A-2252 CF₃ SO₂CH₃ CH₂OCH₃ CH₂CH₂OCH₃ A-2253 CF₃ SO₂CH₃CH₂OCH₂CH₃ CH₃ A-2254 CF₃ SO₂CH₃ CH₂OCH₂CH₃ CH₂CH₃ A-2255 CF₃ SO₂CH₃CH₂OCH₂CH₃ CH₂CH₂CH₃ A-2256 CF₃ SO₂CH₃ CH₂OCH₂CH₃ CH₂CH₂OCH₃ A-2257 CF₃SO₂CH₃ CH₂(CO)OCH₃ CH₃ A-2258 CF₃ SO₂CH₃ CH₂(CO)OCH₃ CH₂CH₃ A-2259 CF₃SO₂CH₃ CH₂(CO)OCH₃ CH₂CH₂CH₃ A-2260 CF₃ SO₂CH₃ CH₂(CO)OCH₃ CH₂CH₂OCH₃A-2261 CF₃ SO₂CH₃ CH₂CHCH₂ CH₃ A-2262 CF₃ SO₂CH₃ CH₂CHCH₂ CH₂CH₃ A-2263CF₃ SO₂CH₃ CH₂CHCH₂ CH₂CH₂CH₃ A-2264 CF₃ SO₂CH₃ CH₂CHCH₂ CH₂CH₂OCH₃A-2265 CF₃ SO₂CH₃ CH₂CCH CH₃ A-2266 CF₃ SO₂CH₃ CH₂CCH CH₂CH₃ A-2267 CF₃SO₂CH₃ CH₂CCH CH₂CH₂CH₃ A-2268 CF₃ SO₂CH₃ CH₂CCH CH₂CH₂OCH₃ A-2269 CF₃SO₂CH₃ CH₂C₆H₅ CH₃ A-2270 CF₃ SO₂CH₃ CH₂C₆H₅ CH₂CH₃ A-2271 CF₃ SO₂CH₃CH₂C₆H₅ CH₂CH₂CH₃ A-2272 CF₃ SO₂CH₃ CH₂C₆H₅ CH₂CH₂OCH₃ A-2273 CF₃ NO₂CH₃ CH₃ A-2274 CF₃ NO₂ CH₃ CH₂CH₃ A-2275 CF₃ NO₂ CH₃ CH₂CH₂CH₃ A-2276CF₃ NO₂ CH₃ CH₂CH₂OCH₃ A-2277 CF₃ NO₂ CH₂CH₃ CH₃ A-2278 CF₃ NO₂ CH₂CH₃CH₂CH₃ A-2279 CF₃ NO₂ CH₂CH₃ CH₂CH₂CH₃ A-2280 CF₃ NO₂ CH₂CH₃ CH₂CH₂OCH₃A-2281 CF₃ NO₂ CH₂OCH₃ CH₃ A-2282 CF₃ NO₂ CH₂OCH₃ CH₂CH₃ A-2283 CF₃ NO₂CH₂OCH₃ CH₂CH₂CH₃ A-2284 CF₃ NO₂ CH₂OCH₃ CH₂CH₂OCH₃ A-2285 CF₃ NO₂CH₂OCH₂CH₃ CH₃ A-2286 CF₃ NO₂ CH₂OCH₂CH₃ CH₂CH₃ A-2287 CF₃ NO₂CH₂OCH₂CH₃ CH₂CH₂CH₃ A-2288 CF₃ NO₂ CH₂OCH₂CH₃ CH₂CH₂OCH₃ A-2289 CF₃ NO₂CH₂(CO)OCH₃ CH₃ A-2290 CF₃ NO₂ CH₂(CO)OCH₃ CH₂CH₃ A-2291 CF₃ NO₂CH₂(CO)OCH₃ CH₂CH₂CH₃ A-2292 CF₃ NO₂ CH₂(CO)OCH₃ CH₂CH₂OCH₃ A-2293 CF₃NO₂ CH₂CHCH₂ CH₃ A-2294 CF₃ NO₂ CH₂CHCH₂ CH₂CH₃ A-2295 CF₃ NO₂ CH₂CHCH₂CH₂CH₂CH₃ A-2296 CF₃ NO₂ CH₂CHCH₂ CH₂CH₂OCH₃ A-2297 CF₃ NO₂ CH₂CCH CH₃A-2298 CF₃ NO₂ CH₂CCH CH₂CH₃ A-2299 CF₃ NO₂ CH₂CCH CH₂CH₂CH₃ A-2300 CF₃NO₂ CH₂CCH CH₂CH₂OCH₃ A-2301 CF₃ NO₂ CH₂C₆H₅ CH₃ A-2302 CF₃ NO₂ CH₂C₆H₅CH₂CH₃ A-2303 CF₃ NO₂ CH₂C₆H₅ CH₂CH₂CH₃ A-2304 CF₃ NO₂ CH₂C₆H₅CH₂CH₂OCH₃

Examples of preferred compounds I.B, where X is CR², are the individualcompounds compiled in Tables 21 to 480 below. Moreover, the meaningsmentioned below for the individual variables in the Tables are per se,independently of the combination in which they are mentioned, aparticularly preferred embodiment of the substituents in question.

Table 21 Compounds of formula I.B1 (I.B1-1.1-I.B1-1.2304) in which B isCH, R² is SCH₃, R⁴ is H and R⁵ is F and the combination of R¹, R³, R⁶and R⁷ for a compound corresponds in each case to one row of Table A;Table 22 Compounds of formula I.B1 (I.B1-2.1-I.B1-2.2304) in which B isCH, R² is SCH₃, R⁴ is H and R⁵ is Cl and the combination of R¹, R³, R⁶and R⁷ for a compound corresponds in each case to one row of Table A;Table 23 Compounds of formula I.B1 (I.B1-3.1-I.B1-3.2304) in which B isCH, R² is SCH₃, R⁴ is F and R⁵ is F and the combination of R¹, R³, R⁶and R⁷ for a compound corresponds in each case to one row of Table A;Table 24 Compounds of formula I.B1 (I.B1-4.1-I.B1-4.2304) in which B isCH, R² is SCH₃, R⁴ is F and R⁵ is Cl and the combination of R¹, R³, R⁶and R⁷ for a compound corresponds in each case to one row of Table A;Table 25 Compounds of formula I.B1 (I.B1-5.1-I.B1-5.2304) in which B isCH, R² is SCH₃, R⁴ is Cl and R⁵ is F and the combination of R¹, R³, R⁶and R⁷ for a compound corresponds in each case to one row of Table A;Table 26 Compounds of formula I.B1 (I.B1-6.1-I.B1-6.2304) in which B isCH, R² is SCH₃, R⁴ is Cl and R⁵ is Cl and the combination of R¹, R³, R⁶and R⁷ for a compound corresponds in each case to one row of Table A;Table 27 Compounds of formula I.B1 (I.B1-7.1-I.B1-7.2304) in which B isCH, R² is SCH₃, R⁴ is CN and R⁵ is F and the combination of R¹, R³, R⁶and R⁷ for a compound corresponds in each case to one row of Table A;Table 28 Compounds of formula I.B1 (I.B1-8.1-I.B1-8.2304) in which B isCH, R² is SCH₃, R⁴ is CN and R⁵ is Cl and the combination of R¹, R³, R⁶and R⁷ for a compound corresponds in each case to one row of Table A;Table 29 Compounds of formula I.B1 (I.B1-9.1-I.B1-9.2304) in which B isCH, R² is SCH₃, R⁴ is CH₃ and R⁵ is F and the combination of R¹, R³, R⁶and R⁷ for a compound corresponds in each case to one row of Table A;Table 30 Compounds of formula I.B1 (I.B1-10.1-I.B1-10.2304) in which Bis CH, R² is SCH₃, R⁴ is CH₃ and R⁵ is Cl and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 31 Compounds of formula I.B2 (I.B2-1.1-I.B2-1.2304) in which B isCH, R² is SCH₂CH₃, R⁴ is H and R⁵ is F and the combination of R¹, R³, R⁶and R⁷ for a compound corresponds in each case to one row of Table A;Table 32 Compounds of formula I.B2 (I.B2-2.1-I.B2-2.2304) in which B isCH, R² is SCH₂CH₃, R⁴ is H and R⁵ is Cl and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 33 Compounds of formula I.B2 (I.B2-3.1-I.B2-3.2304) in which B isCH, R² is SCH₂CH₃, R⁴ is F and R⁵ is F and the combination of R¹, R³, R⁶and R⁷ for a compound corresponds in each case to one row of Table A;Table 34 Compounds of formula I.B2 (I.B2-4.1-I.B2-4.2304) in which B isCH, R² is SCH₂CH₃, R⁴ is F and R⁵ is Cl and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 35 Compounds of formula I.B2 (I.B2-5.1-I.B2-5.2304) in which B isCH, R² is SCH₂CH₃, R⁴ is Cl and R⁵ is F and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 36 Compounds of formula I.B2 (I.B2-6.1-I.B2-6.2304) in which B isCH, R² is SCH₂CH₃, R⁴ is Cl and R⁵ is Cl and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 37 Compounds of formula I.B2 (I.B2-7.1-I.B2-7.2304) in which B isCH, R² is SCH₂CH₃, R⁴ is CN and R⁵ is F and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 38 Compounds of formula I.B2 (I.B2-8.1-I.B2-8.2304) in which B isCH, R² is SCH₂CH₃, R⁴ is CN and R⁵ is Cl and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 39 Compounds of formula I.B2 (I.B2-9.1-I.B2-9.2304) in which B isCH, R² is SCH₂CH₃, R⁴ is CH₃ and R⁵ is F and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 40 Compounds of formula I.B2 (I.B2-10.1-I.B2-10.2304) in which Bis CH, R² is SCH₂CH₃, R⁴ is CH₃ and R⁵ is Cl and the combination of R¹,R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 41 Compounds of formula I.B3 (I.B3-1.1-I.B3-1.2304) in which B isCH, R² is SO₂CH₂CH₃, R⁴ is H and R⁵ is F and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 42 Compounds of formula I.B3 (I.B3-2.1-I.B3-2.2304) in which B isCH, R² is SO₂CH₂CH₃, R⁴ is H and R⁵ is Cl and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 43 Compounds of formula I.B3 (I.B3-3.1-I.B3-3.2304) in which B isCH, R² is SO₂CH₂CH₃, R⁴ is F and R⁵ is F and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 44 Compounds of formula I.B3 (I.B3-4.1-I.B3-4.2304) in which B isCH, R² is SO₂CH₂CH₃, R⁴ is F and R⁵ is Cl and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 45 Compounds of formula I.B3 (I.B3-5.1-I.B3-5.2304) in which B isCH, R² is SO₂CH₂CH₃, R⁴ is Cl and R⁵ is F and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 46 Compounds of formula I.B3 (I.B3-6.1-I.B3-6.2304) in which B isCH, R² is SO₂CH₂CH₃, R⁴ is Cl and R⁵ is Cl and the combination of R¹,R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 47 Compounds of formula I.B3 (I.B3-7.1-I.B3-7.2304) in which B isCH, R² is SO₂CH₂CH₃, R⁴ is CN and R⁵ is F and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 48 Compounds of formula I.B3 (I.B3-8.1-I.B3-8.2304) in which B isCH, R² is SO₂CH₂CH₃, R⁴ is CN and R⁵ is Cl and the combination of R¹,R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 49 Compounds of formula I.B3 (I.B3-9.1-I.B3-9.2304) in which B isCH, R² is SO₂CH₂CH₃, R⁴ is CH₃ and R⁵ is F and the combination of R¹,R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 50 Compounds of formula I.B3 (I.B3-10.1-I.B3-10.2304) in which Bis CH, R² is SO₂CH₂CH₃, R⁴ is CH₃ and R⁵ is Cl and the combination ofR¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 51 Compounds of formula I.B4 (I.B4-1.1-I.B4-1.2304) in which B isCH, R² is SOCH₃, R⁴ is H and R⁵ is F and the combination of R¹, R³, R⁶and R⁷ for a compound corresponds in each case to one row of Table A;Table 52 Compounds of formula I.B4 (I.B4-2.1-I.B4-2.2304) in which B isCH, R² is SOCH₃, R⁴ is H and R⁵ is Cl and the combination of R¹, R³, R⁶and R⁷ for a compound corresponds in each case to one row of Table A;Table 53 Compounds of formula I.B4 (I.B4-3.1-I.B4-3.2304) in which B isCH, R² is SOCH₃, R⁴ is F and R⁵ is F and the combination of R¹, R³, R⁶and R⁷ for a compound corresponds in each case to one row of Table A;Table 54 Compounds of formula I.B4 (I.B4-4.1-I.B4-4.2304) in which B isCH, R² is SOCH₃, R⁴ is F and R⁵ is Cl and the combination of R¹, R³, R⁶and R⁷ for a compound corresponds in each case to one row of Table A;Table 55 Compounds of formula I.B4 (I.B4-5.1-I.B4-5.2304) in which B isCH, R² is SOCH₃, R⁴ is Cl and R⁵ is F and the combination of R¹, R³, R⁶and R⁷ for a compound corresponds in each case to one row of Table A;Table 56 Compounds of formula I.B4 (I.B4-6.1-I.B4-6.2304) in which B isCH, R² is SOCH₃, R⁴ is Cl and R⁵ is Cl and the combination of R¹, R³, R⁶and R⁷ for a compound corresponds in each case to one row of Table A;Table 57 Compounds of formula I.B4 (I.B4-7.1-I.B4-7.2304) in which B isCH, R² is SOCH₃, R⁴ is CN and R⁵ is F and the combination of R¹, R³, R⁶and R⁷ for a compound corresponds in each case to one row of Table A;Table 58 Compounds of formula I.B4 (I.B4-8.1-I.B4-8.2304) in which B isCH, R² is SOCH₃, R⁴ is CN and R⁵ is Cl and the combination of R¹, R³, R⁶and R⁷ for a compound corresponds in each case to one row of Table A;Table 59 Compounds of formula I.B4 (I.B4-9.1-I.B4-9.2304) in which B isCH, R² is SOCH₃, R⁴ is CH₃ and R⁵ is F and the combination of R¹, R³, R⁶and R⁷ for a compound corresponds in each case to one row of Table A;Table 60 Compounds of formula I.B4 (I.B4-10.1-I.B4-10.2304) in which Bis CH, R² is SOCH₃, R⁴ is CH₃ and R⁵ is Cl and the combination of R¹,R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 61 Compounds of formula I.B5 (I.B5-1.1-I.B5-1.2304) in which B isCH, R² is SOCH₂CH₃, R⁴ is H and R⁵ is F and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 62 Compounds of formula I.B5 (I.B5-2.1-I.B5-2.2304) in which B isCH, R² is SOCH₂CH₃, R⁴ is H and R⁵ is Cl and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 63 Compounds of formula I.B5 (I.B5-3.1-I.B5-3.2304) in which B isCH, R² is SOCH₂CH₃, R⁴ is F and R⁵ is F and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 64 Compounds of formula I.B5 (I.B5-4.1-I.B5-4.2304) in which B isCH, R² is SOCH₂CH₃, R⁴ is F and R⁵ is Cl and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 65 Compounds of formula I.B5 (I.B5-5.1-I.B5-5.2304) in which B isCH, R² is SOCH₂CH₃, R⁴ is Cl and R⁵ is F and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 66 Compounds of formula I.B5 (I.B5-6.1-I.B5-6.2304) in which B isCH, R² is SOCH₂CH₃, R⁴ is Cl and R⁵ is Cl and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 67 Compounds of formula I.B5 (I.B5-7.1-I.B5-7.2304) in which B isCH, R² is SOCH₂CH₃, R⁴ is CN and R⁵ is F and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 68 Compounds of formula I.B5 (I.B5-8.1-I.B5-8.2304) in which B isCH, R² is SOCH₂CH₃, R⁴ is CN and R⁵ is Cl and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 69 Compounds of formula I.B5 (I.B5-9.1-I.B5-9.2304) in which B isCH, R² is SOCH₂CH₃, R⁴ is CH₃ and R⁵ is F and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 70 Compounds of formula I.B5 (I.B5-10.1-I.B5-10.2304) in which Bis CH, R² is SOCH₂CH₃, R⁴ is CH₃ and R⁵ is Cl and the combination of R¹,R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 71 Compounds of formula I.B6 (I.B6-1.1-I.B6-1.2304) in which B isCH, R² is OCH₃, R⁴ is H and R⁵ is F and the combination of R¹, R³, R⁶and R⁷ for a compound corresponds in each case to one row of Table A;Table 72 Compounds of formula I.B6 (I.B6-2.1-I.B6-2.2304) in which B isCH, R² is OCH₃, R⁴ is H and R⁵ is Cl and the combination of R¹, R³, R⁶and R⁷ for a compound corresponds in each case to one row of Table A;Table 73 Compounds of formula I.B6 (I.B6-3.1-I.B6-3.2304) in which B isCH, R² is OCH₃, R⁴ is F and R⁵ is F and the combination of R¹, R³, R⁶and R⁷ for a compound corresponds in each case to one row of Table A;Table 74 Compounds of formula I.B6 (I.B6-4.1-I.B6-4.2304) in which B isCH, R² is OCH₃, R⁴ is F and R⁵ is Cl and the combination of R¹, R³, R⁶and R⁷ for a compound corresponds in each case to one row of Table A;Table 75 Compounds of formula I.B6 (I.B6-5.1-I.B6-5.2304) in which B isCH, R² is OCH₃, R⁴ is Cl and R⁵ is F and the combination of R¹, R³, R⁶and R⁷ for a compound corresponds in each case to one row of Table A;Table 76 Compounds of formula I.B6 (I.B6-6.1-I.B6-6.2304) in which B isCH, R² is OCH₃, R⁴ is Cl and R⁵ is Cl and the combination of R¹, R³, R⁶and R⁷ for a compound corresponds in each case to one row of Table A;Table 77 Compounds of formula I.B6 (I.B6-7.1-I.B6-7.2304) in which B isCH, R² is OCH₃, R⁴ is CN and R⁵ is F and the combination of R¹, R³, R⁶and R⁷ for a compound corresponds in each case to one row of Table A;Table 78 Compounds of formula I.B6 (I.B6-8.1-I.B6-8.2304) in which B isCH, R² is OCH₃, R⁴ is CN and R⁵ is Cl and the combination of R¹, R³, R⁶and R⁷ for a compound corresponds in each case to one row of Table A;Table 79 Compounds of formula I.B6 (I.B6-9.1-I.B6-9.2304) in which B isCH, R² is OCH₃, R⁴ is CH₃ and R⁵ is F and the combination of R¹, R³, R⁶and R⁷ for a compound corresponds in each case to one row of Table A;Table 80 Compounds of formula I.B6 (I.B6-10.1-I.B6-10.2304) in which Bis CH, R² is OCH₃, R⁴ is CH₃ and R⁵ is Cl and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 81 Compounds of formula I.B7 (I.B7-1.1-I.B7-1.2304) in which B isCH, R² is OCH₂CH₃, R⁴ is H and R⁵ is F and the combination of R¹, R³, R⁶and R⁷ for a compound corresponds in each case to one row of Table A;Table 82 Compounds of formula I.B7 (I.B7-2.1-I.B7-2.2304) in which B isCH, R² is OCH₂CH₃, R⁴ is H and R⁵ is Cl and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 83 Compounds of formula I.B7 (I.B7-3.1-I.B7-3.2304) in which B isCH, R² is OCH₂CH₃, R⁴ is F and R⁵ is F and the combination of R¹, R³, R⁶and R⁷ for a compound corresponds in each case to one row of Table A;Table 84 Compounds of formula I.B7 (I.B7-4.1-I.B7-4.2304) in which B isCH, R² is OCH₂CH₃, R⁴ is F and R⁵ is Cl and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 85 Compounds of formula I.B7 (I.B7-5.1-I.B7-5.2304) in which B isCH, R² is OCH₂CH₃, R⁴ is Cl and R⁵ is F and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 86 Compounds of formula I.B7 (I.B7-6.1-I.B7-6.2304) in which B isCH, R² is OCH₂CH₃, R⁴ is Cl and R⁵ is Cl and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 87 Compounds of formula I.B7 (I.B7-7.1-I.B7-7.2304) in which B isCH, R² is OCH₂CH₃, R⁴ is CN and R⁵ is F and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 88 Compounds of formula I.B7 (I.B7-8.1-I.B7-8.2304) in which B isCH, R² is OCH₂CH₃, R⁴ is CN and R⁵ is Cl and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 89 Compounds of formula I.B7 (I.B7-9.1-I.B7-9.2304) in which B isCH, R² is OCH₂CH₃, R⁴ is CH₃ and R⁵ is F and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 90 Compounds of formula I.B7 (I.B7-10.1-I.B7-10.2304) in which Bis CH, R² is OCH₂CH₃, R⁴ is CH₃ and R⁵ is Cl and the combination of R¹,R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 91 Compounds of formula I.B8 (I.B8-1.1-I.B8-1.2304) in which B isCH, R² is OCHF₂, R⁴ is H and R⁵ is F and the combination of R¹, R³, R⁶and R⁷ for a compound corresponds in each case to one row of Table A;Table 92 Compounds of formula I.B8 (I.B8-2.1-I.B8-2.2304) in which B isCH, R² is OCHF₂, R⁴ is H and R⁵ is Cl and the combination of R¹, R³, R⁶and R⁷ for a compound corresponds in each case to one row of Table A;Table 93 Compounds of formula I.B8 (I.B8-3.1-I.B8-3.2304) in which B isCH, R² is OCHF₂, R⁴ is F and R⁵ is F and the combination of R¹, R³, R⁶and R⁷ for a compound corresponds in each case to one row of Table A;Table 94 Compounds of formula I.B8 (I.B8-4.1-I.B8-4.2304) in which B isCH, R² is OCHF₂, R⁴ is F and R⁵ is Cl and the combination of R¹, R³, R⁶and R⁷ for a compound corresponds in each case to one row of Table A;Table 95 Compounds of formula I.B8 (I.B8-5.1-I.B8-5.2304) in which B isCH, R² is OCHF₂, R⁴ is Cl and R⁵ is F and the combination of R¹, R³, R⁶and R⁷ for a compound corresponds in each case to one row of Table A;Table 96 Compounds of formula I.B8 (I.B8-6.1-I.B8-6.2304) in which B isCH, R² is OCHF₂, R⁴ is Cl and R⁵ is Cl and the combination of R¹, R³, R⁶and R⁷ for a compound corresponds in each case to one row of Table A;Table 97 Compounds of formula I.B8 (I.B8-7.1-I.B8-7.2304) in which B isCH, R² is OCHF₂, R⁴ is CN and R⁵ is F and the combination of R¹, R³, R⁶and R⁷ for a compound corresponds in each case to one row of Table A;Table 98 Compounds of formula I.B8 (I.B8-8.1-I.B8-8.2304) in which B isCH, R² is OCHF₂, R⁴ is CN and R⁵ is Cl and the combination of R¹, R³, R⁶and R⁷ for a compound corresponds in each case to one row of Table A;Table 99 Compounds of formula I.B8 (I.B8-9.1-I.B8-9.2304) in which B isCH, R² is OCHF₂, R⁴ is CH₃ and R⁵ is F and the combination of R¹, R³, R⁶and R⁷ for a compound corresponds in each case to one row of Table A;Table 100 Compounds of formula I.B8 (I.B8-10.1-I.B8-10.2304) in which Bis CH, R² is OCHF₂, R⁴ is CH₃ and R⁵ is Cl and the combination of R¹,R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 101 Compounds of formula I.B9 (I.B9-1.1-I.B9-1.2304) in which B isCH, R² is OCH₂CF₃, R⁴ is H and R⁵ is F and the combination of R¹, R³, R⁶and R⁷ for a compound corresponds in each case to one row of Table A;Table 102 Compounds of formula I.B9 (I.B9-2.1-I.B9-2.2304) in which B isCH, R² is OCH₂CF₃, R⁴ is H and R⁵ is Cl and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 103 Compounds of formula I.B9 (I.B9-3.1-I.B9-3.2304) in which B isCH, R² is OCH₂CF₃, R⁴ is F and R⁵ is F and the combination of R¹, R³, R⁶and R⁷ for a compound corresponds in each case to one row of Table A;Table 104 Compounds of formula I.B9 (I.B9-4.1-I.B9-4.2304) in which B isCH, R² is OCH₂CF₃, R⁴ is F and R⁵ is Cl and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 105 Compounds of formula I.B9 (I.B9-5.1-I.B9-5.2304) in which B isCH, R² is OCH₂CF₃, R⁴ is Cl and R⁵ is F and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 106 Compounds of formula I.B9 (I.B9-6.1-I.B9-6.2304) in which B isCH, R² is OCH₂CF₃, R⁴ is Cl and R⁵ is Cl and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 107 Compounds of formula I.B9 (I.B9-7.1-I.B9-7.2304) in which B isCH, R² is OCH₂CF₃, R⁴ is CN and R⁵ is F and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 108 Compounds of formula I.B9 (I.B9-8.1-I.B9-8.2304) in which B isCH, R² is OCH₂CF₃, R⁴ is CN and R⁵ is Cl and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 109 Compounds of formula I.B9 (I.B9-9.1-I.B9-9.2304) in which B isCH, R² is OCH₂CF₃, R⁴ is CH₃ and R⁵ is F and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 110 Compounds of formula I.B9 (I.B9-10.1-I.B9-10.2304) in which Bis CH, R² is OCH₂CF₃, R⁴ is CH₃ and R⁵ is Cl and the combination of R¹,R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 111 Compounds of formula I.B10 (I.B10-1.1-I.B10-1.2304) in which Bis CH, R² is OCH₂CH₂OCH₃, R⁴ is H and R⁵ is F and the combination of R¹,R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 112 Compounds of formula I.B10 (I.B10-2.1-I.B10-2.2304) in which Bis CH, R² is OCH₂CH₂OCH₃, R⁴ is H and R⁵ is Cl and the combination ofR¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 113 Compounds of formula I.B10 (I.B10-3.1-I.B10-3.2304) in which Bis CH, R² is OCH₂CH₂OCH₃, R⁴ is F and R⁵ is F and the combination of R¹,R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 114 Compounds of formula I.B10 (I.B10-4.1-I.B10-4.2304) in which Bis CH, R² is OCH₂CH₂OCH₃, R⁴ is F and R⁵ is Cl and the combination ofR¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 115 Compounds of formula I.B10 (I.B10-5.1-I.B10-5.2304) in which Bis CH, R² is OCH₂CH₂OCH₃, R⁴ is Cl and R⁵ is F and the combination ofR¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 116 Compounds of formula I.B10 (I.B10-6.1-I.B10-6.2304) in which Bis CH, R² is OCH₂CH₂OCH₃, R⁴ is Cl and R⁵ is Cl and the combination ofR¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 117 Compounds of formula I.B10 (I.B10-7.1-I.B10-7.2304) in which Bis CH, R² is OCH₂CH₂OCH₃, R⁴ is CN and R⁵ is F and the combination ofR¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 118 Compounds of formula I.B10 (I.B10-8.1-I.B10-8.2304) in which Bis CH, R² is OCH₂CH₂OCH₃, R⁴ is CN and R⁵ is Cl and the combination ofR¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 119 Compounds of formula I.B10 (I.B10-9.1-I.B10-9.2304) in which Bis CH, R² is OCH₂CH₂OCH₃, R⁴ is CH₃ and R⁵ is F and the combination ofR¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 120 Compounds of formula I.B10 (I.B10-10.1-I.B10-10.2304) in whichB is CH, R² is OCH₂CH₂OCH₃, R⁴ is CH₃ and R⁵ is Cl and the combinationof R¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one rowof Table A;Table 121 Compounds of formula I.B11 (I.B11-1.1-I.B11-1.2304) in which Bis CH, R² is H, R⁴ is H and R⁵ is F and the combination of R¹, R³, R⁶and R⁷ for a compound corresponds in each case to one row of Table A;Table 122 Compounds of formula I.B11 (I.B11-2.1-I.B11-2.2304) in which Bis CH, R² is H, R⁴ is H and R⁵ is Cl and the combination of R¹, R³, R⁶and R⁷ for a compound corresponds in each case to one row of Table A;Table 123 Compounds of formula I.B11 (I.B11-3.1-I.B11-3.2304) in which Bis CH, R² is H, R⁴ is F and R⁵ is F and the combination of R¹, R³, R⁶and R⁷ for a compound corresponds in each case to one row of Table A;Table 124 Compounds of formula I.B11 (I.B11-4.1-I.B11-4.2304) in which Bis CH, R² is H, R⁴ is F and R⁵ is Cl and the combination of R¹, R³, R⁶and R⁷ for a compound corresponds in each case to one row of Table A;Table 125 Compounds of formula I.B11 (I.B11-5.1-I.B11-5.2304) in which Bis CH, R² is H, R⁴ is Cl and R⁵ is F and the combination of R¹, R³, R⁶and R⁷ for a compound corresponds in each case to one row of Table A;Table 126 Compounds of formula I.B11 (I.B11-6.1-I.B11-6.2304) in which Bis CH, R² is H, R⁴ is Cl and R⁵ is Cl and the combination of R¹, R³, R⁶and R⁷ for a compound corresponds in each case to one row of Table A;Table 127 Compounds of formula I.B11 (I.B11-7.1-I.B11-7.2304) in which Bis CH, R² is H, R⁴ is CN and R⁵ is F and the combination of R¹, R³, R⁶and R⁷ for a compound corresponds in each case to one row of Table A;Table 128 Compounds of formula I.B11 (I.B11-8.1-I.B11-8.2304) in which Bis CH, R² is H, R⁴ is CN and R⁵ is Cl and the combination of R¹, R³, R⁶and R⁷ for a compound corresponds in each case to one row of Table A;Table 129 Compounds of formula I.B11 (I.B11-9.1-I.B11-9.2304) in which Bis CH, R² is H, R⁴ is CH₃ and R⁵ is F and the combination of R¹, R³, R⁶and R⁷ for a compound corresponds in each case to one row of Table A;Table 130 Compounds of formula I.B11 (I.B11-10.1-I.B11-10.2304) in whichB is CH, R² is H, R⁴ is CH₃ and R⁵ is Cl and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 131 Compounds of formula I.B12 (I.B12-1.1-I.B12-1.2304) in which Bis CH, R² is SO₂CH₃, R⁴ is H and R⁵ is F and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 132 Compounds of formula I.B12 (I.B12-2.1-I.B12-2.2304) in which Bis CH, R² is SO₂CH₃, R⁴ is H and R⁵ is Cl and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 133 Compounds of formula I.B12 (I.B12-3.1-I.B12-3.2304) in which Bis CH, R² is SO₂CH₃, R⁴ is F and R⁵ is F and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 134 Compounds of formula I.B12 (I.B12-4.1-I.B12-4.2304) in which Bis CH, R² is SO₂CH₃, R⁴ is F and R⁵ is Cl and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 135 Compounds of formula I.B12 (I.B12-5.1-I.B12-5.2304) in which Bis CH, R² is SO₂CH₃, R⁴ is Cl and R⁵ is F and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 136 Compounds of formula I.B12 (I.B12-6.1-I.B12-6.2304) in which Bis CH, R² is SO₂CH₃, R⁴ is Cl and R⁵ is Cl and the combination of R¹,R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 137 Compounds of formula I.B12 (I.B12-7.1-I.B12-7.2304) in which Bis CH, R² is SO₂CH₃, R⁴ is CN and R⁵ is F and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 138 Compounds of formula I.B12 (I.B12-8.1-I.B12-8.2304) in which Bis CH, R² is SO₂CH₃, R⁴ is CN and R⁵ is Cl and the combination of R¹,R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 139 Compounds of formula I.B12 (I.B12-9.1-I.B12-9.2304) in which Bis CH, R² is SO₂CH₃, R⁴ is CH₃ and R⁵ is F and the combination of R¹,R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 140 Compounds of formula I.B12 (I.B12-10.1-I.B12-10.2304) in whichB is CH, R² is SO₂CH₃, R⁴ is CH₃ and R⁵ is Cl and the combination of R¹,R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 141 Compounds of formula I.B13 (I.B13-1.1-I.B13-1.2304) in which Bis CH, R² is CH₂OCH₂CF₃, R⁴ is H and R⁵ is F and the combination of R¹,R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 142 Compounds of formula I.B13 (I.B13-2.1-I.B13-2.2304) in which Bis CH, R² is CH₂OCH₂CF₃, R⁴ is H and R⁵ is Cl and the combination of R¹,R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 143 Compounds of formula I.B13 (I.B13-3.1-I.B13-3.2304) in which Bis CH, R² is CH₂OCH₂CF₃, R⁴ is F and R⁵ is F and the combination of R¹,R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 144 Compounds of formula I.B13 (I.B13-4.1-I.B13-4.2304) in which Bis CH, R² is CH₂OCH₂CF₃, R⁴ is F and R⁵ is Cl and the combination of R¹,R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 145 Compounds of formula I.B13 (I.B13-5.1-I.B13-5.2304) in which Bis CH, R² is CH₂OCH₂CF₃, R⁴ is Cl and R⁵ is F and the combination of R¹,R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 146 Compounds of formula I.B13 (I.B13-6.1-I.B13-6.2304) in which Bis CH, R² is CH₂OCH₂CF₃, R⁴ is Cl and R⁵ is Cl and the combination ofR¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 147 Compounds of formula I.B13 (I.B13-7.1-I.B13-7.2304) in which Bis CH, R² is CH₂OCH₂CF₃, R⁴ is CN and R⁵ is F and the combination of R¹,R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 148 Compounds of formula I.B13 (I.B13-8.1-I.B13-8.2304) in which Bis CH, R² is CH₂OCH₂CF₃, R⁴ is CN and R⁵ is Cl and the combination ofR¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 149 Compounds of formula I.B13 (I.B13-9.1-I.B13-9.2304) in which Bis CH, R² is CH₂OCH₂CF₃, R⁴ is CH₃ and R⁵ is F and the combination ofR¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 150 Compounds of formula I.B13 (I.B13-10.1-I.B13-10.2304) in whichB is CH, R² is CH₂OCH₂CF₃, R⁴ is CH₃ and R⁵ is Cl and the combination ofR¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 151 Compounds of formula I.B14 (I.B14-1.1-I.B14-1.2304) in which Bis CH, R² is isoxazolin-3-yl, R⁴ is H and R⁵ is F and the combination ofR¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 152 Compounds of formula I.B14 (I.B14-2.1-I.B14-2.2304) in which Bis CH, R² is isoxazolin-3-yl, R⁴ is H and R⁵ is Cl and the combinationof R¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one rowof Table A;Table 153 Compounds of formula I.B14 (I.B14-3.1-I.B14-3.2304) in which Bis CH, R² is isoxazolin-3-yl, R⁴ is F and R⁵ is F and the combination ofR¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 154 Compounds of formula I.B14 (I.B14-4.1-I.B14-4.2304) in which Bis CH, R² is isoxazolin-3-yl, R⁴ is F and R⁵ is Cl and the combinationof R¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one rowof Table A;Table 155 Compounds of formula I.B14 (I.B14-5.1-I.B14-5.2304) in which Bis CH, R² is isoxazolin-3-yl, R⁴ is Cl and R⁵ is F and the combinationof R¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one rowof Table A;Table 156 Compounds of formula I.B14 (I.B14-6.1-I.B14-6.2304) in which Bis CH, R² is isoxazolin-3-yl, R⁴ is Cl and R⁵ is Cl and the combinationof R¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one rowof Table A;Table 157 Compounds of formula I.B14 (I.B14-7.1-I.B14-7.2304) in which Bis CH, R² is isoxazolin-3-yl, R⁴ is CN and R⁵ is F and the combinationof R¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one rowof Table A;Table 158 Compounds of formula I.B14 (I.B14-8.1-I.B14-8.2304) in which Bis CH, R² is isoxazolin-3-yl, R⁴ is CN and R⁵ is Cl and the combinationof R¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one rowof Table A;Table 159 Compounds of formula I.B14 (I.B14-9.1-I.B14-9.2304) in which Bis CH, R² is isoxazolin-3-yl, R⁴ is CH₃ and R⁵ is F and the combinationof R¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one rowof Table A;Table 160 Compounds of formula I.B14 (I.B14-10.1-I.B14-10.2304) in whichB is CH, R² is isoxazolin-3-yl, R⁴ is CH₃ and R⁵ is Cl and thecombination of R¹, R³, R⁶ and R⁷ for a compound corresponds in each caseto one row of Table A;Table 161 Compounds of formula I.B15 (I.B15-1.1-I.B15-1.2304) in which Bis CH, R² is 5-methyl-isoxazolin-3-yl, R⁴ is H and R⁵ is F and thecombination of R¹, R³, R⁶ and R⁷ for a compound corresponds in each caseto one row of Table A;Table 162 Compounds of formula I.B15 (I.B15-2.1-I.B15-2.2304) in which Bis CH, R² is 5-methyl-isoxazolin-3-yl, R⁴ is H and R⁵ is Cl and thecombination of R¹, R³, R⁶ and R⁷ for a compound corresponds in each caseto one row of Table A;Table 163 Compounds of formula I.B15 (I.B15-3.1-I.B15-3.2304) in which Bis CH, R² is 5-methyl-isoxazolin-3-yl, R⁴ is F and R⁵ is F and thecombination of R¹, R³, R⁶ and R⁷ for a compound corresponds in each caseto one row of Table A;Table 164 Compounds of formula I.B15 (I.B15-4.1-I.B15-4.2304) in which Bis CH, R² is 5-methyl-isoxazolin-3-yl, R⁴ is F and R⁵ is Cl and thecombination of R¹, R³, R⁶ and R⁷ for a compound corresponds in each caseto one row of Table A;Table 165 Compounds of formula I.B15 (I.B15-5.1-I.B15-5.2304) in which Bis CH, R² is 5-methyl-isoxazolin-3-yl, R⁴ is Cl and R⁵ is F and thecombination of R¹, R³, R⁶ and R⁷ for a compound corresponds in each caseto one row of Table A;Table 166 Compounds of formula I.B15 (I.B15-6.1-I.B15-6.2304) in which Bis CH, R² is 5-methyl-isoxazolin-3-yl, R⁴ is Cl and R⁵ is Cl and thecombination of R¹, R³, R⁶ and R⁷ for a compound corresponds in each caseto one row of Table A;Table 167 Compounds of formula I.B15 (I.B15-7.1-I.B15-7.2304) in which Bis CH, R² is 5-methyl-isoxazolin-3-yl, R⁴ is CN and R⁵ is F and thecombination of R¹, R³, R⁶ and R⁷ for a compound corresponds in each caseto one row of Table A;Table 168 Compounds of formula I.B15 (I.B15-8.1-I.B15-8.2304) in which Bis CH, R² is 5-methyl-isoxazolin-3-yl, R⁴ is CN and R⁵ is Cl and thecombination of R¹, R³, R⁶ and R⁷ for a compound corresponds in each caseto one row of Table A;Table 169 Compounds of formula I.B15 (I.B15-9.1-I.B15-9.2304) in which Bis CH, R² is 5-methyl-isoxazolin-3-yl, R⁴ is CH₃ and R⁵ is F and thecombination of R¹, R³, R⁶ and R⁷ for a compound corresponds in each caseto one row of Table A;Table 170 Compounds of formula I.B15 (I.B15-10.1-I.B15-10.2304) in whichB is CH, R² is 5-methyl-isoxazolin-3-yl, R⁴ is CH₃ and R⁵ is Cl and thecombination of R¹, R³, R⁶ and R⁷ for a compound corresponds in each caseto one row of Table A;Table 171 Compounds of formula I.B16 (I.B16-1.1-I.B16-1.2304) in which Bis CH, R² is isoxazol-3-yl, R⁴ is H and R⁵ is F and the combination ofR¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 172 Compounds of formula I.B16 (I.B16-2.1-I.B16-2.2304) in which Bis CH, R² is isoxazol-3-yl, R⁴ is H and R⁵ is Cl and the combination ofR¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 173 Compounds of formula I.B16 (I.B16-3.1-I.B16-3.2304) in which Bis CH, R² is isoxazol-3-yl, R⁴ is F and R⁵ is F and the combination ofR¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 174 Compounds of formula I.B16 (I.B16-4.1-I.B16-4.2304) in which Bis CH, R² is isoxazol-3-yl, R⁴ is F and R⁵ is Cl and the combination ofR¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 175 Compounds of formula I.B16 (I.B16-5.1-I.B16-5.2304) in which Bis CH, R² is isoxazol-3-yl, R⁴ is Cl and R⁵ is F and the combination ofR¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 176 Compounds of formula I.B16 (I.B16-6.1-I.B16-6.2304) in which Bis CH, R² is isoxazol-3-yl, R⁴ is Cl and R⁵ is Cl and the combination ofR¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 177 Compounds of formula I.B16 (I.B16-7.1-I.B16-7.2304) in which Bis CH, R² is isoxazol-3-yl, R⁴ is CN and R⁵ is F and the combination ofR¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 178 Compounds of formula I.B16 (I.B16-8.1-I.B16-8.2304) in which Bis CH, R² is isoxazol-3-yl, R⁴ is CN and R⁵ is Cl and the combination ofR¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 179 Compounds of formula I.B16 (I.B16-9.1-I.B16-9.2304) in which Bis CH, R² is isoxazol-3-yl, R⁴ is CH₃ and R⁵ is F and the combination ofR¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 180 Compounds of formula I.B16 (I.B16-10.1-I.B16-10.2304) in whichB is CH, R² is isoxazol-3-yl, R⁴ is CH₃ and R⁵ is Cl and the combinationof R¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one rowof Table A;Table 181 Compounds of formula I.B17 (I.B17-1.1-I.B17-1.2304) in which Bis CH, R² is 5-methyl-isoxazol-3-yl, R⁴ is H and R⁵ is F and thecombination of R¹, R³, R⁶ and R⁷ for a compound corresponds in each caseto one row of Table A;Table 182 Compounds of formula I.B17 (I.B17-2.1-I.B17-2.2304) in which Bis CH, R² is 5-methyl-isoxazol-3-yl, R⁴ is H and R⁵ is Cl and thecombination of R¹, R³, R⁶ and R⁷ for a compound corresponds in each caseto one row of Table A;Table 183 Compounds of formula I.B17 (I.B17-3.1-I.B17-3.2304) in which Bis CH, R² is 5-methyl-isoxazol-3-yl, R⁴ is F and R⁵ is F and thecombination of R¹, R³, R⁶ and R⁷ for a compound corresponds in each caseto one row of Table A;Table 184 Compounds of formula I.B17 (I.B17-4.1-I.B17-4.2304) in which Bis CH, R² is 5-methyl-isoxazol-3-yl, R⁴ is F and R⁵ is Cl and thecombination of R¹, R³, R⁶ and R⁷ for a compound corresponds in each caseto one row of Table A;Table 185 Compounds of formula I.B17 (I.B17-5.1-I.B17-5.2304) in which Bis CH, R² is 5-methyl-isoxazol-3-yl, R⁴ is Cl and R⁵ is F and thecombination of R¹, R³, R⁶ and R⁷ for a compound corresponds in each caseto one row of Table A;Table 186 Compounds of formula I.B17 (I.B17-6.1-I.B17-6.2304) in which Bis CH, R² is 5-methyl-isoxazol-3-yl, R⁴ is Cl and R⁵ is Cl and thecombination of R¹, R³, R⁶ and R⁷ for a compound corresponds in each caseto one row of Table A;Table 187 Compounds of formula I.B17 (I.B17-7.1-I.B17-7.2304) in which Bis CH, R² is 5-methyl-isoxazol-3-yl, R⁴ is CN and R⁵ is F and thecombination of R¹, R³, R⁶ and R⁷ for a compound corresponds in each caseto one row of Table A;Table 188 Compounds of formula I.B17 (I.B17-8.1-I.B17-8.2304) in which Bis CH, R² is 5-methyl-isoxazol-3-yl, R⁴ is CN and R⁵ is Cl and thecombination of R¹, R³, R⁶ and R⁷ for a compound corresponds in each caseto one row of Table A;Table 189 Compounds of formula I.B17 (I.B17-9.1-I.B17-9.2304) in which Bis CH, R² is 5-methyl-isoxazol-3-yl, R⁴ is CH₃ and R⁵ is F and thecombination of R¹, R³, R⁶ and R⁷ for a compound corresponds in each caseto one row of Table A;Table 190 Compounds of formula I.B17 (I.B17-10.1-I.B17-10.2304) in whichB is CH, R² is 5-methyl-isoxazol-3-yl, R⁴ is CH₃ and R⁵ is Cl and thecombination of R¹, R³, R⁶ and R⁷ for a compound corresponds in each caseto one row of Table A;Table 191 Compounds of formula I.B18 (I.B18-1.1-I.B18-1.2304) in which Bis CH, R² is 3-methyl-isoxazolin-5-yl, R⁴ is H and R⁵ is F and thecombination of R¹, R³, R⁶ and R⁷ for a compound corresponds in each caseto one row of Table A;Table 192 Compounds of formula I.B18 (I.B18-2.1-I.B18-2.2304) in which Bis CH, R² is 3-methyl-isoxazolin-5-yl, R⁴ is H and R⁵ is Cl and thecombination of R¹, R³, R⁶ and R⁷ for a compound corresponds in each caseto one row of Table A;Table 193 Compounds of formula I.B18 (I.B18-3.1-I.B18-3.2304) in which Bis CH, R² is 3-methyl-isoxazolin-5-yl, R⁴ is F and R⁵ is F and thecombination of R¹, R³, R⁶ and R⁷ for a compound corresponds in each caseto one row of Table A;Table 194 Compounds of formula I.B18 (I.B18-4.1-I.B18-4.2304) in which Bis CH, R² is 3-methyl-isoxazolin-5-yl, R⁴ is F and R⁵ is Cl and thecombination of R¹, R³, R⁶ and R⁷ for a compound corresponds in each caseto one row of Table A;Table 195 Compounds of formula I.B18 (I.B18-5.1-I.B18-5.2304) in which Bis CH, R² is 3-methyl-isoxazolin-5-yl, R⁴ is Cl and R⁵ is F and thecombination of R¹, R³, R⁶ and R⁷ for a compound corresponds in each caseto one row of Table A;Table 196 Compounds of formula I.B18 (I.B18-6.1-I.B18-6.2304) in which Bis CH, R² is 3-methyl-isoxazolin-5-yl, R⁴ is Cl and R⁵ is Cl and thecombination of R¹, R³, R⁶ and R⁷ for a compound corresponds in each caseto one row of Table A;Table 197 Compounds of formula I.B18 (I.B18-7.1-I.B18-7.2304) in which Bis CH, R² is 3-methyl-isoxazolin-5-yl, R⁴ is CN and R⁵ is F and thecombination of R¹, R³, R⁶ and R⁷ for a compound corresponds in each caseto one row of Table A;Table 198 Compounds of formula I.B18 (I.B18-8.1-I.B18-8.2304) in which Bis CH, R² is 3-methyl-isoxazolin-5-yl, R⁴ is CN and R⁵ is Cl and thecombination of R¹, R³, R⁶ and R⁷ for a compound corresponds in each caseto one row of Table A;Table 199 Compounds of formula I.B18 (I.B18-9.1-I.B18-9.2304) in which Bis CH, R² is 3-methyl-isoxazolin-5-yl, R⁴ is CH₃ and R⁵ is F and thecombination of R¹, R³, R⁶ and R⁷ for a compound corresponds in each caseto one row of Table A;Table 200 Compounds of formula I.B18 (I.B18-10.1-I.B18-10.2304) in whichB is CH, R² is 3-methyl-isoxazolin-5-yl, R⁴ is CH₃ and R⁵ is Cl and thecombination of R¹, R³, R⁶ and R⁷ for a compound corresponds in each caseto one row of Table A;Table 201 Compounds of formula I.B19 (I.B19-1.1-I.B19-1.2304) in which Bis CH, R² is 3-methyl-isoxazol-5-yl, R⁴ is H and R⁵ is F and thecombination of R¹, R³, R⁶ and R⁷ for a compound corresponds in each caseto one row of Table A;Table 202 Compounds of formula I.B19 (I.B19-2.1-I.B19-2.2304) in which Bis CH, R² is 3-methyl-isoxazol-5-yl, R⁴ is H and R⁵ is Cl and thecombination of R¹, R³, R⁶ and R⁷ for a compound corresponds in each caseto one row of Table A;Table 203 Compounds of formula I.B19 (I.B19-3.1-I.B19-3.2304) in which Bis CH, R² is 3-methyl-isoxazol-5-yl, R⁴ is F and R⁵ is F and thecombination of R¹, R³, R⁶ and R⁷ for a compound corresponds in each caseto one row of Table A;Table 204 Compounds of formula I.B19 (I.B19-4.1-I.B19-4.2304) in which Bis CH, R² is 3-methyl-isoxazol-5-yl, R⁴ is F and R⁵ is Cl and thecombination of R¹, R³, R⁶ and R⁷ for a compound corresponds in each caseto one row of Table A;Table 205 Compounds of formula I.B19 (I.B19-5.1-I.B19-5.2304) in which Bis CH, R² is 3-methyl-isoxazol-5-yl, R⁴ is Cl and R⁵ is F and thecombination of R¹, R³, R⁶ and R⁷ for a compound corresponds in each caseto one row of Table A;Table 206 Compounds of formula I.B19 (I.B19-6.1-I.B19-6.2304) in which Bis CH, R² is 3-methyl-isoxazol-5-yl, R⁴ is Cl and R⁵ is Cl and thecombination of R¹, R³, R⁶ and R⁷ for a compound corresponds in each caseto one row of Table A;Table 207 Compounds of formula I.B19 (I.B19-7.1-I.B19-7.2304) in which Bis CH, R² is 3-methyl-isoxazol-5-yl, R⁴ is CN and R⁵ is F and thecombination of R¹, R³, R⁶ and R⁷ for a compound corresponds in each caseto one row of Table A;Table 208 Compounds of formula I.B19 (I.B19-8.1-I.B19-8.2304) in which Bis CH, R² is 3-methyl-isoxazol-5-yl, R⁴ is CN and R⁵ is Cl and thecombination of R¹, R³, R⁶ and R⁷ for a compound corresponds in each caseto one row of Table A;Table 209 Compounds of formula I.B19 (I.B19-9.1-I.B19-9.2304) in which Bis CH, R² is 3-methyl-isoxazol-5-yl, R⁴ is CH₃ and R⁵ is F and thecombination of R¹, R³, R⁶ and R⁷ for a compound corresponds in each caseto one row of Table A;Table 210 Compounds of formula I.B19 (I.B19-10.1-I.B19-10.2304) in whichB is CH, R² is 3-methyl-isoxazol-5-yl, R⁴ is CH₃ and R⁵ is Cl and thecombination of R¹, R³, R⁶ and R⁷ for a compound corresponds in each caseto one row of Table A;Table 211 Compounds of formula I.B20 (I.B20-1.1-I.B20-1.2304) in which Bis CH, R² is CH₃, R⁴ is H and R⁵ is F and the combination of R¹, R³, R⁶and R⁷ for a compound corresponds in each case to one row of Table A;Table 212 Compounds of formula I.B20 (I.B20-2.1-I.B20-2.2304) in which Bis CH, R² is CH₃, R⁴ is H and R⁵ is Cl and the combination of R¹, R³, R⁶and R⁷ for a compound corresponds in each case to one row of Table A;Table 213 Compounds of formula I.B20 (I.B20-3.1-I.B20-3.2304) in which Bis CH, R² is CH₃, R⁴ is F and R⁵ is F and the combination of R¹, R³, R⁶and R⁷ for a compound corresponds in each case to one row of Table A;Table 214 Compounds of formula I.B20 (I.B20-4.1-I.B20-4.2304) in which Bis CH, R² is CH₃, R⁴ is F and R⁵ is Cl and the combination of R¹, R³, R⁶and R⁷ for a compound corresponds in each case to one row of Table A;Table 215 Compounds of formula I.B20 (I.B20-5.1-I.B20-5.2304) in which Bis CH, R² is CH₃, R⁴ is Cl and R⁵ is F and the combination of R¹, R³, R⁶and R⁷ for a compound corresponds in each case to one row of Table A;Table 216 Compounds of formula I.B20 (I.B20-6.1-I.B20-6.2304) in which Bis CH, R² is CH₃, R⁴ is Cl and R⁵ is Cl and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 217 Compounds of formula I.B20 (I.B20-7.1-I.B20-7.2304) in which Bis CH, R² is CH₃, R⁴ is CN and R⁵ is F and the combination of R¹, R³, R⁶and R⁷ for a compound corresponds in each case to one row of Table A;Table 218 Compounds of formula I.B20 (I.B20-8.1-I.B20-8.2304) in which Bis CH, R² is CH₃, R⁴ is CN and R⁵ is Cl and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 219 Compounds of formula I.B20 (I.B20-9.1-I.B20-9.2304) in which Bis CH, R² is CH₃, R⁴ is CH₃ and R⁵ is F and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 220 Compounds of formula I.B20 (I.B20-10.1-I.B20-10.2304) in whichB is CH, R² is CH₃, R⁴ is CH₃ and R⁵ is Cl and the combination of R¹,R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 221 Compounds of formula I.B21 (I.B21-1.1-I.B21-1.2304) in which Bis CH, R² is CH₂OCH₃, R⁴ is H and R⁵ is F and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 222 Compounds of formula I.B21 (I.B21-2.1-I.B21-2.2304) in which Bis CH, R² is CH₂OCH₃, R⁴ is H and R⁵ is Cl and the combination of R¹,R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 223 Compounds of formula I.B21 (I.B21-3.1-I.B21-3.2304) in which Bis CH, R² is CH₂OCH₃, R⁴ is F and R⁵ is F and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 224 Compounds of formula I.B21 (I.B21-4.1-I.B21-4.2304) in which Bis CH, R² is CH₂OCH₃, R⁴ is F and R⁵ is Cl and the combination of R¹,R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 225 Compounds of formula I.B21 (I.B21-5.1-I.B21-5.2304) in which Bis CH, R² is CH₂OCH₃, R⁴ is Cl and R⁵ is F and the combination of R¹,R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 226 Compounds of formula I.B21 (I.B21-6.1-I.B21-6.2304) in which Bis CH, R² is CH₂OCH₃, R⁴ is Cl and R⁵ is Cl and the combination of R¹,R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 227 Compounds of formula I.B21 (I.B21-7.1-I.B21-7.2304) in which Bis CH, R² is CH₂OCH₃, R⁴ is CN and R⁵ is F and the combination of R¹,R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 228 Compounds of formula I.B21 (I.B21-8.1-I.B21-8.2304) in which Bis CH, R² is CH₂OCH₃, R⁴ is CN and R⁵ is Cl and the combination of R¹,R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 229 Compounds of formula I.B21 (I.B21-9.1-I.B21-9.2304) in which Bis CH, R² is CH₂OCH₃, R⁴ is CH₃ and R⁵ is F and the combination of R¹,R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 230 Compounds of formula I.B21 (I.B21-10.1-I.B21-10.2304) in whichB is CH, R² is CH₂OCH₃, R⁴ is CH₃ and R⁵ is Cl and the combination ofR¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 231 Compounds of formula I.B22 (I.B22-1.1-I.B22-1.2304) in which Bis CH, R² is OCH₂CH(CH₂)₂, R⁴ is H and R⁵ is F and the combination ofR¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 232 Compounds of formula I.B22 (I.B22-2.1-I.B22-2.2304) in which Bis CH, R² is OCH₂CH(CH₂)₂, R⁴ is H and R⁵ is Cl and the combination ofR¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 233 Compounds of formula I.B22 (I.B22-3.1-I.B22-3.2304) in which Bis CH, R² is OCH₂CH(CH₂)₂, R⁴ is F and R⁵ is F and the combination ofR¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 234 Compounds of formula I.B22 (I.B22-4.1-I.B22-4.2304) in which Bis CH, R² is OCH₂CH(CH₂)₂, R⁴ is F and R⁵ is Cl and the combination ofR¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 235 Compounds of formula I.B22 (I.B22-5.1-I.B22-5.2304) in which Bis CH, R² is OCH₂CH(CH₂)₂, R⁴ is Cl and R⁵ is F and the combination ofR¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 236 Compounds of formula I.B22 (I.B22-6.1-I.B22-6.2304) in which Bis CH, R² is OCH₂CH(CH₂)₂, R⁴ is Cl and R⁵ is Cl and the combination ofR¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 237 Compounds of formula I.B22 (I.B22-7.1-I.B22-7.2304) in which Bis CH, R² is OCH₂CH(CH₂)₂, R⁴ is CN and R⁵ is F and the combination ofR¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 238 Compounds of formula I.B22 (I.B22-8.1-I.B22-8.2304) in which Bis CH, R² is OCH₂CH(CH₂)₂, R⁴ is CN and R⁵ is Cl and the combination ofR¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 239 Compounds of formula I.B22 (I.B22-9.1-I.B22-9.2304) in which Bis CH, R² is OCH₂CH(CH₂)₂, R⁴ is CH₃ and R⁵ is F and the combination ofR¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 240 Compounds of formula I.B22 (I.B22-10.1-I.B22-10.2304) in whichB is CH, R² is OCH₂CH(CH₂)₂, R⁴ is CH₃ and R⁵ is Cl and the combinationof R¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one rowof Table A;Table 241 Compounds of formula I.B23 (I.B23-1.1-I.B23-1.2304) in which Bis CH, R² is NCH₃SO₂CH₃, R⁴ is H and R⁵ is F and the combination of R¹,R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 242 Compounds of formula I.B23 (I.B23-2.1-I.B23-2.2304) in which Bis CH, R² is NCH₃SO₂CH₃, R⁴ is H and R⁵ is Cl and the combination of R¹,R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 243 Compounds of formula I.B23 (I.B23-3.1-I.B23-3.2304) in which Bis CH, R² is NCH₃SO₂CH₃, R⁴ is F and R⁵ is F and the combination of R¹,R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 244 Compounds of formula I.B23 (I.B23-4.1-I.B23-4.2304) in which Bis CH, R² is NCH₃SO₂CH₃, R⁴ is F and R⁵ is Cl and the combination of R¹,R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 245 Compounds of formula I.B23 (I.B23-5.1-I.B23-5.2304) in which Bis CH, R² is NCH₃SO₂CH₃, R⁴ is Cl and R⁵ is F and the combination of R¹,R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 246 Compounds of formula I.B23 (I.B23-6.1-I.B23-6.2304) in which Bis CH, R² is NCH₃SO₂CH₃, R⁴ is Cl and R⁵ is Cl and the combination ofR¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 247 Compounds of formula I.B23 (I.B23-7.1-I.B23-7.2304) in which Bis CH, R² is NCH₃SO₂CH₃, R⁴ is CN and R⁵ is F and the combination of R¹,R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 248 Compounds of formula I.B23 (I.B23-8.1-I.B23-8.2304) in which Bis CH, R² is NCH₃SO₂CH₃, R⁴ is CN and R⁵ is Cl and the combination ofR¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 249 Compounds of formula I.B23 (I.B23-9.1-I.B23-9.2304) in which Bis CH, R² is NCH₃SO₂CH₃, R⁴ is CH₃ and R⁵ is F and the combination ofR¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 250 Compounds of formula I.B23 (I.B23-10.1-I.B23-10.2304) in whichB is CH, R² is NCH₃SO₂CH₃, R⁴ is CH₃ and R⁵ is Cl and the combination ofR¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 251 Compounds of formula I.B1 (I.B1-11.1-I.B1-11.2304) in which Bis N, R² is SCH₃, R⁴ is H and R⁵ is F and the combination of R¹, R³, R⁶and R⁷ for a compound corresponds in each case to one row of Table A;Table 252 Compounds of formula I.B1 (I.B1-12.1-I.B1-12.2304) in which Bis N, R² is SCH₃, R⁴ is H and R⁵ is Cl and the combination of R¹, R³, R⁶and R⁷ for a compound corresponds in each case to one row of Table A;Table 253 Compounds of formula I.B1 (I.B1-13.1-I.B1-13.2304) in which Bis N, R² is SCH₃, R⁴ is F and R⁵ is F and the combination of R¹, R³, R⁶and R⁷ for a compound corresponds in each case to one row of Table A;Table 254 Compounds of formula I.B1 (I.B1-14.1-I.B1-14.2304) in which Bis N, R² is SCH₃, R⁴ is F and R⁵ is Cl and the combination of R¹, R³, R⁶and R⁷ for a compound corresponds in each case to one row of Table A;Table 255 Compounds of formula I.B1 (I.B1-15.1-I.B1-15.2304) in which Bis N, R² is SCH₃, R⁴ is Cl and R⁵ is F and the combination of R¹, R³, R⁶and R⁷ for a compound corresponds in each case to one row of Table A;Table 256 Compounds of formula I.B1 (I.B1-16.1-I.B1-16.2304) in which Bis N, R² is SCH₃, R⁴ is Cl and R⁵ is Cl and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 257 Compounds of formula I.B1 (I.B1-17.1-I.B1-17.2304) in which Bis N, R² is SCH₃, R⁴ is CN and R⁵ is F and the combination of R¹, R³, R⁶and R⁷ for a compound corresponds in each case to one row of Table A;Table 258 Compounds of formula I.B1 (I.B1-18.1-I.B1-18.2304) in which Bis N, R² is SCH₃, R⁴ is CN and R⁵ is Cl and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 259 Compounds of formula I.B1 (I.B1-19.1-I.B1-19.2304) in which Bis N, R² is SCH₃, R⁴ is CH₃ and R⁵ is F and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 260 Compounds of formula I.B1 (I.B1-20.1-I.B1-20.2304) in which Bis N, R² is SCH₃, R⁴ is CH₃ and R⁵ is Cl and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 261 Compounds of formula I.B2 (I.B2-11.1-I.B2-11.2304) in which Bis N, R² is SCH₂CH₃, R⁴ is H and R⁵ is F and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 262 Compounds of formula I.B2 (I.B2-12.1-I.B2-12.2304) in which Bis N, R² is SCH₂CH₃, R⁴ is H and R⁵ is Cl and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 263 Compounds of formula I.B2 (I.B2-13.1-I.B2-13.2304) in which Bis N, R² is SCH₂CH₃, R⁴ is F and R⁵ is F and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 264 Compounds of formula I.B2 (I.B2-14.1-I.B2-14.2304) in which Bis N, R² is SCH₂CH₃, R⁴ is F and R⁵ is Cl and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 265 Compounds of formula I.B2 (I.B2-15.1-I.B2-15.2304) in which Bis N, R² is SCH₂CH₃, R⁴ is Cl and R⁵ is F and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 266 Compounds of formula I.B2 (I.B2-16.1-I.B2-16.2304) in which Bis N, R² is SCH₂CH₃, R⁴ is Cl and R⁵ is Cl and the combination of R¹,R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 267 Compounds of formula I.B2 (I.B2-17.1-I.B2-17.2304) in which Bis N, R² is SCH₂CH₃, R⁴ is CN and R⁵ is F and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 268 Compounds of formula I.B2 (I.B2-18.1-I.B2-18.2304) in which Bis N, R² is SCH₂CH₃, R⁴ is CN and R⁵ is Cl and the combination of R¹,R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 269 Compounds of formula I.B2 (I.B2-19.1-I.B2-19.2304) in which Bis N, R² is SCH₂CH₃, R⁴ is CH₃ and R⁵ is F and the combination of R¹,R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 270 Compounds of formula I.B2 (I.B2-20.1-I.B2-20.2304) in which Bis N, R² is SCH₂CH₃, R⁴ is CH₃ and R⁵ is Cl and the combination of R¹,R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 271 Compounds of formula I.B3 (I.B3-11.1-I.B3-11.2304) in which Bis N, R² is SO₂CH₂CH₃, R⁴ is H and R⁵ is F and the combination of R¹,R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 272 Compounds of formula I.B3 (I.B3-12.1-I.B3-12.2304) in which Bis N, R² is SO₂CH₂CH₃, R⁴ is H and R⁵ is Cl and the combination of R¹,R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 273 Compounds of formula I.B3 (I.B3-13.1-I.B3-13.2304) in which Bis N, R² is SO₂CH₂CH₃, R⁴ is F and R⁵ is F and the combination of R¹,R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 274 Compounds of formula I.B3 (I.B3-14.1-I.B3-14.2304) in which Bis N, R² is SO₂CH₂CH₃, R⁴ is F and R⁵ is Cl and the combination of R¹,R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 275 Compounds of formula I.B3 (I.B3-15.1-I.B3-15.2304) in which Bis N, R² is SO₂CH₂CH₃, R⁴ is Cl and R⁵ is F and the combination of R¹,R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 276 Compounds of formula I.B3 (I.B3-16.1-I.B3-16.2304) in which Bis N, R² is SO₂CH₂CH₃, R⁴ is Cl and R⁵ is Cl and the combination of R¹,R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 277 Compounds of formula I.B3 (I.B3-17.1-I.B3-17.2304) in which Bis N, R² is SO₂CH₂CH₃, R⁴ is CN and R⁵ is F and the combination of R¹,R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 278 Compounds of formula I.B3 (I.B3-18.1-I.B3-18.2304) in which Bis N, R² is SO₂CH₂CH₃, R⁴ is CN and R⁵ is Cl and the combination of R¹,R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 279 Compounds of formula I.B3 (I.B3-19.1-I.B3-19.2304) in which Bis N, R² is SO₂CH₂CH₃, R⁴ is CH₃ and R⁵ is F and the combination of R¹,R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 280 Compounds of formula I.B3 (I.B3-20.1-I.B3-20.2304) in which Bis N, R² is SO₂CH₂CH₃, R⁴ is CH₃ and R⁵ is Cl and the combination of R¹,R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 281 Compounds of formula I.B4 (I.B4-11.1-I.B4-11.2304) in which Bis N, R² is SOCH₃, R⁴ is H and R⁵ is F and the combination of R¹, R³, R⁶and R⁷ for a compound corresponds in each case to one row of Table A;Table 282 Compounds of formula I.B4 (I.B4-12.1-I.B4-12.2304) in which Bis N, R² is SOCH₃, R⁴ is H and R⁵ is Cl and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 283 Compounds of formula I.B4 (I.B4-13.1-I.B4-13.2304) in which Bis N, R² is SOCH₃, R⁴ is F and R⁵ is F and the combination of R¹, R³, R⁶and R⁷ for a compound corresponds in each case to one row of Table A;Table 284 Compounds of formula I.B4 (I.B4-14.1-I.B4-14.2304) in which Bis N, R² is SOCH₃, R⁴ is F and R⁵ is Cl and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 285 Compounds of formula I.B4 (I.B4-15.1-I.B4-15.2304) in which Bis N, R² is SOCH₃, R⁴ is Cl and R⁵ is F and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 286 Compounds of formula I.B4 (I.B4-16.1-I.B4-16.2304) in which Bis N, R² is SOCH₃, R⁴ is Cl and R⁵ is Cl and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 287 Compounds of formula I.B4 (I.B4-17.1-I.B4-17.2304) in which Bis N, R² is SOCH₃, R⁴ is CN and R⁵ is F and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 288 Compounds of formula I.B4 (I.B4-18.1-I.B4-18.2304) in which Bis N, R² is SOCH₃, R⁴ is CN and R⁵ is Cl and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 289 Compounds of formula I.B4 (I.B4-19.1-I.B4-19.2304) in which Bis N, R² is SOCH₃, R⁴ is CH₃ and R⁵ is F and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 290 Compounds of formula I.B4 (I.B4-20.1-I.B4-20.2304) in which Bis N, R² is SOCH₃, R⁴ is CH₃ and R⁵ is Cl and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 291 Compounds of formula I.B5 (I.B5-11.1-I.B5-11.2304) in which Bis N, R² is SOCH₂CH₃, R⁴ is H and R⁵ is F and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 292 Compounds of formula I.B5 (I.B5-12.1-I.B5-12.2304) in which Bis N, R² is SOCH₂CH₃, R⁴ is H and R⁵ is Cl and the combination of R¹,R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 293 Compounds of formula I.B5 (I.B5-13.1-I.B5-13.2304) in which Bis N, R² is SOCH₂CH₃, R⁴ is F and R⁵ is F and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 294 Compounds of formula I.B5 (I.B5-14.1-I.B5-14.2304) in which Bis N, R² is SOCH₂CH₃, R⁴ is F and R⁵ is Cl and the combination of R¹,R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 295 Compounds of formula I.B5 (I.B5-15.1-I.B5-15.2304) in which Bis N, R² is SOCH₂CH₃, R⁴ is Cl and R⁵ is F and the combination of R¹,R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 296 Compounds of formula I.B5 (I.B5-16.1-I.B5-16.2304) in which Bis N, R² is SOCH₂CH₃, R⁴ is Cl and R⁵ is Cl and the combination of R¹,R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 297 Compounds of formula I.B5 (I.B5-17.1-I.B5-17.2304) in which Bis N, R² is SOCH₂CH₃, R⁴ is CN and R⁵ is F and the combination of R¹,R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 298 Compounds of formula I.B5 (I.B5-18.1-I.B5-18.2304) in which Bis N, R² is SOCH₂CH₃, R⁴ is CN and R⁵ is Cl and the combination of R¹,R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 299 Compounds of formula I.B5 (I.B5-19.1-I.B5-19.2304) in which Bis N, R² is SOCH₂CH₃, R⁴ is CH₃ and R⁵ is F and the combination of R¹,R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 300 Compounds of formula I.B5 (I.B5-20.1-I.B5-20.2304) in which Bis N, R² is SOCH₂CH₃, R⁴ is CH₃ and R⁵ is Cl and the combination of R¹,R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 301 Compounds of formula I.B6 (I.B6-11.1-I.B6-11.2304) in which Bis N, R² is OCH₃, R⁴ is H and R⁵ is F and the combination of R¹, R³, R⁶and R⁷ for a compound corresponds in each case to one row of Table A;Table 302 Compounds of formula I.B6 (I.B6-12.1-I.B6-12.2304) in which Bis N, R² is OCH₃, R⁴ is H and R⁵ is Cl and the combination of R¹, R³, R⁶and R⁷ for a compound corresponds in each case to one row of Table A;Table 303 Compounds of formula I.B6 (I.B6-13.1-I.B6-13.2304) in which Bis N, R² is OCH₃, R⁴ is F and R⁵ is F and the combination of R¹, R³, R⁶and R⁷ for a compound corresponds in each case to one row of Table A;Table 304 Compounds of formula I.B6 (I.B6-14.1-I.B6-14.2304) in which Bis N, R² is OCH₃, R⁴ is F and R⁵ is Cl and the combination of R¹, R³, R⁶and R⁷ for a compound corresponds in each case to one row of Table A;Table 305 Compounds of formula I.B6 (I.B6-15.1-I.B6-15.2304) in which Bis N, R² is OCH₃, R⁴ is Cl and R⁵ is F and the combination of R¹, R³, R⁶and R⁷ for a compound corresponds in each case to one row of Table A;Table 306 Compounds of formula I.B6 (I.B6-16.1-I.B6-16.2304) in which Bis N, R² is OCH₃, R⁴ is Cl and R⁵ is Cl and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 307 Compounds of formula I.B6 (I.B6-17.1-I.B6-17.2304) in which Bis N, R² is OCH₃, R⁴ is CN and R⁵ is F and the combination of R¹, R³, R⁶and R⁷ for a compound corresponds in each case to one row of Table A;Table 308 Compounds of formula I.B6 (I.B6-18.1-I.B6-18.2304) in which Bis N, R² is OCH₃, R⁴ is CN and R⁵ is Cl and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 309 Compounds of formula I.B6 (I.B6-19.1-I.B6-19.2304) in which Bis N, R² is OCH₃, R⁴ is CH₃ and R⁵ is F and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 310 Compounds of formula I.B6 (I.B6-20.1-I.B6-20.2304) in which Bis N, R² is OCH₃, R⁴ is CH₃ and R⁵ is Cl and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 311 Compounds of formula I.B7 (I.B7-11.1-I.B7-11.2304) in which Bis N, R² is OCH₂CH₃, R⁴ is H and R⁵ is F and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 312 Compounds of formula I.B7 (I.B7-12.1-I.B7-12.2304) in which Bis N, R² is OCH₂CH₃, R⁴ is H and R⁵ is Cl and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 313 Compounds of formula I.B7 (I.B7-13.1-I.B7-13.2304) in which Bis N, R² is OCH₂CH₃, R⁴ is F and R⁵ is F and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 314 Compounds of formula I.B7 (I.B7-14.1-I.B7-14.2304) in which Bis N, R² is OCH₂CH₃, R⁴ is F and R⁵ is Cl and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 315 Compounds of formula I.B7 (I.B7-15.1-I.B7-15.2304) in which Bis N, R² is OCH₂CH₃, R⁴ is Cl and R⁵ is F and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 316 Compounds of formula I.B7 (I.B7-16.1-I.B7-16.2304) in which Bis N, R² is OCH₂CH₃, R⁴ is Cl and R⁵ is Cl and the combination of R¹,R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 317 Compounds of formula I.B7 (I.B7-17.1-I.B7-17.2304) in which Bis N, R² is OCH₂CH₃, R⁴ is CN and R⁵ is F and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 318 Compounds of formula I.B7 (I.B7-18.1-I.B7-18.2304) in which Bis N, R² is OCH₂CH₃, R⁴ is CN and R⁵ is Cl and the combination of R¹,R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 319 Compounds of formula I.B7 (I.B7-19.1-I.B7-19.2304) in which Bis N, R² is OCH₂CH₃, R⁴ is CH₃ and R⁵ is F and the combination of R¹,R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 320 Compounds of formula I.B7 (I.B7-20.1-I.B7-20.2304) in which Bis N, R² is OCH₂CH₃, R⁴ is CH₃ and R⁵ is Cl and the combination of R¹,R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 321 Compounds of formula I.B8 (I.B8-11.1-I.B8-11.2304) in which Bis N, R² is OCHF₂, R⁴ is H and R⁵ is F and the combination of R¹, R³, R⁶and R⁷ for a compound corresponds in each case to one row of Table A;Table 322 Compounds of formula I.B8 (I.B8-12.1-I.B8-12.2304) in which Bis N, R² is OCHF₂, R⁴ is H and R⁵ is Cl and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 323 Compounds of formula I.B8 (I.B8-13.1-I.B8-13.2304) in which Bis N, R² is OCHF₂, R⁴ is F and R⁵ is F and the combination of R¹, R³, R⁶and R⁷ for a compound corresponds in each case to one row of Table A;Table 324 Compounds of formula I.B8 (I.B8-14.1-I.B8-14.2304) in which Bis N, R² is OCHF₂, R⁴ is F and R⁵ is Cl and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 325 Compounds of formula I.B8 (I.B8-15.1-I.B8-15.2304) in which Bis N, R² is OCHF₂, R⁴ is Cl and R⁵ is F and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 326 Compounds of formula I.B8 (I.B8-16.1-I.B8-16.2304) in which Bis N, R² is OCHF₂, R⁴ is Cl and R⁵ is Cl and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 327 Compounds of formula I.B8 (I.B8-17.1-I.B8-17.2304) in which Bis N, R² is OCHF₂, R⁴ is CN and R⁵ is F and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 328 Compounds of formula I.B8 (I.B8-18.1-I.B8-18.2304) in which Bis N, R² is OCHF₂, R⁴ is CN and R⁵ is Cl and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 329 Compounds of formula I.B8 (I.B8-19.1-I.B8-19.2304) in which Bis N, R² is OCHF₂, R⁴ is CH₃ and R⁵ is F and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 330 Compounds of formula I.B8 (I.B8-20.1-I.B8-20.2304) in which Bis N, R² is OCHF₂, R⁴ is CH₃ and R⁵ is Cl and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 331 Compounds of formula I.B9 (I.B9-11.1-I.B9-11.2304) in which Bis N, R² is OCH₂CF₃, R⁴ is H and R⁵ is F and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 332 Compounds of formula I.B9 (I.B9-12.1-I.B9-12.2304) in which Bis N, R² is OCH₂CF₃, R⁴ is H and R⁵ is Cl and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 333 Compounds of formula I.B9 (I.B9-13.1-I.B9-13.2304) in which Bis N, R² is OCH₂CF₃, R⁴ is F and R⁵ is F and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 334 Compounds of formula I.B9 (I.B9-14.1-I.B9-14.2304) in which Bis N, R² is OCH₂CF₃, R⁴ is F and R⁵ is Cl and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 335 Compounds of formula I.B9 (I.B9-15.1-I.B9-15.2304) in which Bis N, R² is OCH₂CF₃, R⁴ is Cl and R⁵ is F and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 336 Compounds of formula I.B9 (I.B9-16.1-I.B9-16.2304) in which Bis N, R² is OCH₂CF₃, R⁴ is Cl and R⁵ is Cl and the combination of R¹,R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 337 Compounds of formula I.B9 (I.B9-17.1-I.B9-17.2304) in which Bis N, R² is OCH₂CF₃, R⁴ is CN and R⁵ is F and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 338 Compounds of formula I.B9 (I.B9-18.1-I.B9-18.2304) in which Bis N, R² is OCH₂CF₃, R⁴ is CN and R⁵ is Cl and the combination of R¹,R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 339 Compounds of formula I.B9 (I.B9-19.1-I.B9-19.2304) in which Bis N, R² is OCH₂CF₃, R⁴ is CH₃ and R⁵ is F and the combination of R¹,R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 340 Compounds of formula I.B9 (I.B9-20.1-I.B9-20.2304) in which Bis N, R² is OCH₂CF₃, R⁴ is CH₃ and R⁵ is Cl and the combination of R¹,R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 341 Compounds of formula I.B10 (I.B10-11.1-I.B10-11.2304) in whichB is N, R² is OCH₂CH₂OCH₃, R⁴ is H and R⁵ is F and the combination ofR¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 342 Compounds of formula I.B10 (I.B10-12.1-I.B10-12.2304) in whichB is N, R² is OCH₂CH₂OCH₃, R⁴ is H and R⁵ is Cl and the combination ofR¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 343 Compounds of formula I.B10 (I.B10-13.1-I.B10-13.2304) in whichB is N, R² is OCH₂CH₂OCH₃, R⁴ is F and R⁵ is F and the combination ofR¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 344 Compounds of formula I.B10 (I.B10-14.1-I.B10-14.2304) in whichB is N, R² is OCH₂CH₂OCH₃, R⁴ is F and R⁵ is Cl and the combination ofR¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 345 Compounds of formula I.B10 (I.B10-15.1-I.B10-15.2304) in whichB is N, R² is OCH₂CH₂OCH₃, R⁴ is Cl and R⁵ is F and the combination ofR¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 346 Compounds of formula I.B10 (I.B10-16.1-I.B10-16.2304) in whichB is N, R² is OCH₂CH₂OCH₃, R⁴ is Cl and R⁵ is Cl and the combination ofR¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 347 Compounds of formula I.B10 (I.B10-17.1-I.B10-17.2304) in whichB is N, R² is OCH₂CH₂OCH₃, R⁴ is CN and R⁵ is F and the combination ofR¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 348 Compounds of formula I.B10 (I.B10-18.1-I.B10-18.2304) in whichB is N, R² is OCH₂CH₂OCH₃, R⁴ is CN and R⁵ is Cl and the combination ofR¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 349 Compounds of formula I.B10 (I.B10-19.1-I.B10-19.2304) in whichB is N, R² is OCH₂CH₂OCH₃, R⁴ is CH₃ and R⁵ is F and the combination ofR¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 350 Compounds of formula I.B10 (I.B10-20.1-I.B10-20.2304) in whichB is N, R² is OCH₂CH₂OCH₃, R⁴ is CH₃ and R⁵ is Cl and the combination ofR¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 351 Compounds of formula I.B11 (I.B11-11.1-I.B11-11.2304) in whichB is N, R² is H, R⁴ is H and R⁵ is F and the combination of R¹, R³, R⁶and R⁷ for a compound corresponds in each case to one row of Table A;Table 352 Compounds of formula I.B11 (I.B11-12.1-I.B11-12.2304) in whichB is N, R² is H, R⁴ is H and R⁵ is Cl and the combination of R¹, R³, R⁶and R⁷ for a compound corresponds in each case to one row of Table A;Table 353 Compounds of formula I.B11 (I.B11-13.1-I.B11-13.2304) in whichB is N, R² is H, R⁴ is F and R⁵ is F and the combination of R¹, R³, R⁶and R⁷ for a compound corresponds in each case to one row of Table A;Table 354 Compounds of formula I.B11 (I.B11-14.1-I.B11-14.2304) in whichB is N, R² is H, R⁴ is F and R⁵ is Cl and the combination of R¹, R³, R⁶and R⁷ for a compound corresponds in each case to one row of Table A;Table 355 Compounds of formula I.B11 (I.B11-15.1-I.B11-15.2304) in whichB is N, R² is H, R⁴ is Cl and R⁵ is F and the combination of R¹, R³, R⁶and R⁷ for a compound corresponds in each case to one row of Table A;Table 356 Compounds of formula I.B11 (I.B11-16.1-I.B11-16.2304) in whichB is N, R² is H, R⁴ is Cl and R⁵ is Cl and the combination of R¹, R³, R⁶and R⁷ for a compound corresponds in each case to one row of Table A;Table 357 Compounds of formula I.B11 (I.B11-17.1-I.B11-17.2304) in whichB is N, R² is H, R⁴ is CN and R⁵ is F and the combination of R¹, R³, R⁶and R⁷ for a compound corresponds in each case to one row of Table A;Table 358 Compounds of formula I.B11 (I.B11-18.1-I.B11-18.2304) in whichB is N, R² is H, R⁴ is CN and R⁵ is Cl and the combination of R¹, R³, R⁶and R⁷ for a compound corresponds in each case to one row of Table A;Table 359 Compounds of formula I.B11 (I.B11-19.1-I.B11-19.2304) in whichB is N, R² is H, R⁴ is CH₃ and R⁵ is F and the combination of R¹, R³, R⁶and R⁷ for a compound corresponds in each case to one row of Table A;Table 360 Compounds of formula I.B11 (I.B11-20.1-I.B11-20.2304) in whichB is N, R² is H, R⁴ is CH₃ and R⁵ is Cl and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 361 Compounds of formula I.B12 (I.B12-11.1-I.B12-11.2304) in whichB is N, R² is SO₂CH₃, R⁴ is H and R⁵ is F and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 362 Compounds of formula I.B12 (I.B12-12.1-I.B12-12.2304) in whichB is N, R² is SO₂CH₃, R⁴ is H and R⁵ is Cl and the combination of R¹,R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 363 Compounds of formula I.B12 (I.B12-13.1-I.B12-13.2304) in whichB is N, R² is SO₂CH₃, R⁴ is F and R⁵ is F and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 364 Compounds of formula I.B12 (I.B12-14.1-I.B12-14.2304) in whichB is N, R² is SO₂CH₃, R⁴ is F and R⁵ is Cl and the combination of R¹,R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 365 Compounds of formula I.B12 (I.B12-15.1-I.B12-15.2304) in whichB is N, R² is SO₂CH₃, R⁴ is Cl and R⁵ is F and the combination of R¹,R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 366 Compounds of formula I.B12 (I.B12-16.1-I.B12-16.2304) in whichB is N, R² is SO₂CH₃, R⁴ is Cl and R⁵ is Cl and the combination of R¹,R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 367 Compounds of formula I.B12 (I.B12-17.1-I.B12-17.2304) in whichB is N, R² is SO₂CH₃, R⁴ is CN and R⁵ is F and the combination of R¹,R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 368 Compounds of formula I.B12 (I.B12-18.1-I.B12-18.2304) in whichB is N, R² is SO₂CH₃, R⁴ is CN and R⁵ is Cl and the combination of R¹,R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 369 Compounds of formula I.B12 (I.B12-19.1-I.B12-19.2304) in whichB is N, R² is SO₂CH₃, R⁴ is CH₃ and R⁵ is F and the combination of R¹,R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 370 Compounds of formula I.B12 (I.B12-20.1-I.B12-20.2304) in whichB is N, R² is SO₂CH₃, R⁴ is CH₃ and R⁵ is Cl and the combination of R¹,R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 371 Compounds of formula I.B13 (I.B13-11.1-I.B13-11.2304) in whichB is N, R² is CH₂OCH₂CF₃, R⁴ is H and R⁵ is F and the combination of R¹,R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 372 Compounds of formula I.B13 (I.B13-12.1-I.B13-12.2304) in whichB is N, R² is CH₂OCH₂CF₃, R⁴ is H and R⁵ is Cl and the combination ofR¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 373 Compounds of formula I.B13 (I.B13-13.1-I.B13-13.2304) in whichB is N, R² is CH₂OCH₂CF₃, R⁴ is F and R⁵ is F and the combination of R¹,R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 374 Compounds of formula I.B13 (I.B13-14.1-I.B13-14.2304) in whichB is N, R² is CH₂OCH₂CF₃, R⁴ is F and R⁵ is Cl and the combination ofR¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 375 Compounds of formula I.B13 (I.B13-15.1-I.B13-15.2304) in whichB is N, R² is CH₂OCH₂CF₃, R⁴ is Cl and R⁵ is F and the combination ofR¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 376 Compounds of formula I.B13 (I.B13-16.1-I.B13-16.2304) in whichB is N, R² is CH₂OCH₂CF₃, R⁴ is Cl and R⁵ is Cl and the combination ofR¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 377 Compounds of formula I.B13 (I.B13-17.1-I.B13-17.2304) in whichB is N, R² is CH₂OCH₂CF₃, R⁴ is CN and R⁵ is F and the combination ofR¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 378 Compounds of formula I.B13 (I.B13-18.1-I.B13-18.2304) in whichB is N, R² is CH₂OCH₂CF₃, R⁴ is CN and R⁵ is Cl and the combination ofR¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 379 Compounds of formula I.B13 (I.B13-19.1-I.B13-19.2304) in whichB is N, R² is CH₂OCH₂CF₃, R⁴ is CH₃ and R⁵ is F and the combination ofR¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 380 Compounds of formula I.B13 (I.B13-20.1-I.B13-20.2304) in whichB is N, R² is CH₂OCH₂CF₃, R⁴ is CH₃ and R⁵ is Cl and the combination ofR¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 381 Compounds of formula I.B14 (I.B14-11.1-I.B14-11.2304) in whichB is N, R² is isoxazolin-3-yl, R⁴ is H and R⁵ is F and the combinationof R¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one rowof Table A;Table 382 Compounds of formula I.B14 (I.B14-12.1-I.B14-12.2304) in whichB is N, R² is isoxazolin-3-yl, R⁴ is H and R⁵ is Cl and the combinationof R¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one rowof Table A;Table 383 Compounds of formula I.B14 (I.B14-13.1-I.B14-13.2304) in whichB is N, R² is isoxazolin-3-yl, R⁴ is F and R⁵ is F and the combinationof R¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one rowof Table A;Table 384 Compounds of formula I.B14 (I.B14-14.1-I.B14-14.2304) in whichB is N, R² is isoxazolin-3-yl, R⁴ is F and R⁵ is Cl and the combinationof R¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one rowof Table A;Table 385 Compounds of formula I.B14 (I.B14-15.1-I.B14-15.2304) in whichB is N, R² is isoxazolin-3-yl, R⁴ is Cl and R⁵ is F and the combinationof R¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one rowof Table A;Table 386 Compounds of formula I.B14 (I.B14-16.1-I.B14-16.2304) in whichB is N, R² is isoxazolin-3-yl, R⁴ is Cl and R⁵ is Cl and the combinationof R¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one rowof Table A;Table 387 Compounds of formula I.B14 (I.B14-17.1-I.B14-17.2304) in whichB is N, R² is isoxazolin-3-yl, R⁴ is CN and R⁵ is F and the combinationof R¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one rowof Table A;Table 388 Compounds of formula I.B14 (I.B14-18.1-I.B14-18.2304) in whichB is N, R² is isoxazolin-3-yl, R⁴ is CN and R⁵ is Cl and the combinationof R¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one rowof Table A;Table 389 Compounds of formula I.B14 (I.B14-19.1-I.B14-19.2304) in whichB is N, R² is isoxazolin-3-yl, R⁴ is CH₃ and R⁵ is F and the combinationof R¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one rowof Table A;Table 390 Compounds of formula I.B14 (I.B14-20.1-I.B14-20.2304) in whichB is N, R² is isoxazolin-3-yl, R⁴ is CH₃ and R⁵ is Cl and thecombination of R¹, R³, R⁶ and R⁷ for a compound corresponds in each caseto one row of Table A;Table 391 Compounds of formula I.B15 (I.B15-11.1-I.B15-11.2304) in whichB is N, R² is 5-methyl-isoxazolin-3-yl, R⁴ is H and R⁵ is F and thecombination of R¹, R³, R⁶ and R⁷ for a compound corresponds in each caseto one row of Table A;Table 392 Compounds of formula I.B15 (I.B15-12.1-I.B15-12.2304) in whichB is N, R² is 5-methyl-isoxazolin-3-yl, R⁴ is H and R⁵ is Cl and thecombination of R¹, R³, R⁶ and R⁷ for a compound corresponds in each caseto one row of Table A;Table 393 Compounds of formula I.B15 (I.B15-13.1-I.B15-13.2304) in whichB is N, R² is 5-methyl-isoxazolin-3-yl, R⁴ is F and R⁵ is F and thecombination of R¹, R³, R⁶ and R⁷ for a compound corresponds in each caseto one row of Table A;Table 394 Compounds of formula I.B15 (I.B15-14.1-I.B15-14.2304) in whichB is N, R² is 5-methyl-isoxazolin-3-yl, R⁴ is F and R⁵ is Cl and thecombination of R¹, R³, R⁶ and R⁷ for a compound corresponds in each caseto one row of Table A;Table 395 Compounds of formula I.B15 (I.B15-15.1-I.B15-15.2304) in whichB is N, R² is 5-methyl-isoxazolin-3-yl, R⁴ is Cl and R⁵ is F and thecombination of R¹, R³, R⁶ and R⁷ for a compound corresponds in each caseto one row of Table A;Table 396 Compounds of formula I.B15 (I.B15-16.1-I.B15-16.2304) in whichB is N, R² is 5-methyl-isoxazolin-3-yl, R⁴ is Cl and R⁵ is Cl and thecombination of R¹, R³, R⁶ and R⁷ for a compound corresponds in each caseto one row of Table A;Table 397 Compounds of formula I.B15 (I.B15-17.1-I.B15-17.2304) in whichB is N, R² is 5-methyl-isoxazolin-3-yl, R⁴ is CN and R⁵ is F and thecombination of R¹, R³, R⁶ and R⁷ for a compound corresponds in each caseto one row of Table A;Table 398 Compounds of formula I.B15 (I.B15-18.1-I.B15-18.2304) in whichB is N, R² is 5-methyl-isoxazolin-3-yl, R⁴ is CN and R⁵ is Cl and thecombination of R¹, R³, R⁶ and R⁷ for a compound corresponds in each caseto one row of Table A;Table 399 Compounds of formula I.B15 (I.B15-19.1-I.B15-19.2304) in whichB is N, R² is 5-methyl-isoxazolin-3-yl, R⁴ is CH₃ and R⁵ is F and thecombination of R¹, R³, R⁶ and R⁷ for a compound corresponds in each caseto one row of Table A;Table 400 Compounds of formula I.B15 (I.B15-20.1-I.B15-20.2304) in whichB is N, R² is 5-methyl-isoxazolin-3-yl, R⁴ is CH₃ and R⁵ is Cl and thecombination of R¹, R³, R⁶ and R⁷ for a compound corresponds in each caseto one row of Table A;Table 401 Compounds of formula I.B16 (I.B16-11.1-I.B16-11.2304) in whichB is N, R² is isoxazol-3-yl, R⁴ is H and R⁵ is F and the combination ofR¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 402 Compounds of formula I.B16 (I.B16-12.1-I.B16-12.2304) in whichB is N, R² is isoxazol-3-yl, R⁴ is H and R⁵ is Cl and the combination ofR¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 403 Compounds of formula I.B16 (I.B16-13.1-I.B16-13.2304) in whichB is N, R² is isoxazol-3-yl, R⁴ is F and R⁵ is F and the combination ofR¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 404 Compounds of formula I.B16 (I.B16-14.1-I.B16-14.2304) in whichB is N, R² is isoxazol-3-yl, R⁴ is F and R⁵ is Cl and the combination ofR¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 405 Compounds of formula I.B16 (I.B16-15.1-I.B16-15.2304) in whichB is N, R² is isoxazol-3-yl, R⁴ is Cl and R⁵ is F and the combination ofR¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 406 Compounds of formula I.B16 (I.B16-16.1-I.B16-16.2304) in whichB is N, R² is isoxazol-3-yl, R⁴ is Cl and R⁵ is Cl and the combinationof R¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one rowof Table A;Table 407 Compounds of formula I.B16 (I.B16-17.1-I.B16-17.2304) in whichB is N, R² is isoxazol-3-yl, R⁴ is CN and R⁵ is F and the combination ofR¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 408 Compounds of formula I.B16 (I.B16-18.1-I.B16-18.2304) in whichB is N, R² is isoxazol-3-yl, R⁴ is CN and R⁵ is Cl and the combinationof R¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one rowof Table A;Table 409 Compounds of formula I.B16 (I.B16-19.1-I.B16-19.2304) in whichB is N, R² is isoxazol-3-yl, R⁴ is CH₃ and R⁵ is F and the combinationof R¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one rowof Table A;Table 410 Compounds of formula I.B16 (I.B16-20.1-I.B16-20.2304) in whichB is N, R² is isoxazol-3-yl, R⁴ is CH₃ and R⁵ is Cl and the combinationof R¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one rowof Table A;Table 411 Compounds of formula I.B17 (I.B17-11.1-I.B17-11.2304) in whichB is N, R² is 5-methyl-isoxazol-3-yl, R⁴ is H and R⁵ is F and thecombination of R¹, R³, R⁶ and R⁷ for a compound corresponds in each caseto one row of Table A;Table 412 Compounds of formula I.B17 (I.B17-12.1-I.B17-12.2304) in whichB is N, R² is 5-methyl-isoxazol-3-yl, R⁴ is H and R⁵ is Cl and thecombination of R¹, R³, R⁶ and R⁷ for a compound corresponds in each caseto one row of Table A;Table 413 Compounds of formula I.B17 (I.B17-13.1-I.B17-13.2304) in whichB is N, R² is 5-methyl-isoxazol-3-yl, R⁴ is F and R⁵ is F and thecombination of R¹, R³, R⁶ and R⁷ for a compound corresponds in each caseto one row of Table A;Table 414 Compounds of formula I.B17 (I.B17-14.1-I.B17-14.2304) in whichB is N, R² is 5-methyl-isoxazol-3-yl, R⁴ is F and R⁵ is Cl and thecombination of R¹, R³, R⁶ and R⁷ for a compound corresponds in each caseto one row of Table A;Table 415 Compounds of formula I.B17 (I.B17-15.1-I.B17-15.2304) in whichB is N, R² is 5-methyl-isoxazol-3-yl, R⁴ is Cl and R⁵ is F and thecombination of R¹, R³, R⁶ and R⁷ for a compound corresponds in each caseto one row of Table A;Table 416 Compounds of formula I.B17 (I.B17-16.1-I.B17-16.2304) in whichB is N, R² is 5-methyl-isoxazol-3-yl, R⁴ is Cl and R⁵ is Cl and thecombination of R¹, R³, R⁶ and R⁷ for a compound corresponds in each caseto one row of Table A;Table 417 Compounds of formula I.B17 (I.B17-17.1-I.B17-17.2304) in whichB is N, R² is 5-methyl-isoxazol-3-yl, R⁴ is CN and R⁵ is F and thecombination of R¹, R³, R⁶ and R⁷ for a compound corresponds in each caseto one row of Table A;Table 418 Compounds of formula I.B17 (I.B17-18.1-I.B17-18.2304) in whichB is N, R² is 5-methyl-isoxazol-3-yl, R⁴ is CN and R⁵ is Cl and thecombination of R¹, R³, R⁶ and R⁷ for a compound corresponds in each caseto one row of Table A;Table 419 Compounds of formula I.B17 (I.B17-19.1-I.B17-19.2304) in whichB is N, R² is 5-methyl-isoxazol-3-yl, R⁴ is CH₃ and R⁵ is F and thecombination of R¹, R³, R⁶ and R⁷ for a compound corresponds in each caseto one row of Table A;Table 420 Compounds of formula I.B17 (I.B17-20.1-I.B17-20.2304) in whichB is N, R² is 5-methyl-isoxazol-3-yl, R⁴ is CH₃ and R⁵ is Cl and thecombination of R¹, R³, R⁶ and R⁷ for a compound corresponds in each caseto one row of Table A;Table 421 Compounds of formula I.B18 (I.B18-11.1-I.B18-11.2304) in whichB is N, R² is 3-methyl-isoxazolin-5-yl, R⁴ is H and R⁵ is F and thecombination of R¹, R³, R⁶ and R⁷ for a compound corresponds in each caseto one row of Table A;Table 422 Compounds of formula I.B18 (I.B18-12.1-I.B18-12.2304) in whichB is N, R² is 3-methyl-isoxazolin-5-yl, R⁴ is H and R⁵ is Cl and thecombination of R¹, R³, R⁶ and R⁷ for a compound corresponds in each caseto one row of Table A;Table 423 Compounds of formula I.B18 (I.B18-13.1-I.B18-13.2304) in whichB is N, R² is 3-methyl-isoxazolin-5-yl, R⁴ is F and R⁵ is F and thecombination of R¹, R³, R⁶ and R⁷ for a compound corresponds in each caseto one row of Table A;Table 424 Compounds of formula I.B18 (I.B18-14.1-I.B18-14.2304) in whichB is N, R² is 3-methyl-isoxazolin-5-yl, R⁴ is F and R⁵ is Cl and thecombination of R¹, R³, R⁶ and R⁷ for a compound corresponds in each caseto one row of Table A;Table 425 Compounds of formula I.B18 (I.B18-15.1-I.B18-15.2304) in whichB is N, R² is 3-methyl-isoxazolin-5-yl, R⁴ is Cl and R⁵ is F and thecombination of R¹, R³, R⁶ and R⁷ for a compound corresponds in each caseto one row of Table A;Table 426 Compounds of formula I.B18 (I.B18-16.1-I.B18-16.2304) in whichB is N, R² is 3-methyl-isoxazolin-5-yl, R⁴ is Cl and R⁵ is Cl and thecombination of R¹, R³, R⁶ and R⁷ for a compound corresponds in each caseto one row of Table A;Table 427 Compounds of formula I.B18 (I.B18-17.1-I.B18-17.2304) in whichB is N, R² is 3-methyl-isoxazolin-5-yl, R⁴ is CN and R⁵ is F and thecombination of R¹, R³, R⁶ and R⁷ for a compound corresponds in each caseto one row of Table A;Table 428 Compounds of formula I.B18 (I.B18-18.1-I.B18-18.2304) in whichB is N, R² is 3-methyl-isoxazolin-5-yl, R⁴ is CN and R⁵ is Cl and thecombination of R¹, R³, R⁶ and R⁷ for a compound corresponds in each caseto one row of Table A;Table 429 Compounds of formula I.B18 (I.B18-19.1-I.B18-19.2304) in whichB is N, R² is 3-methyl-isoxazolin-5-yl, R⁴ is CH₃ and R⁵ is F and thecombination of R¹, R³, R⁶ and R⁷ for a compound corresponds in each caseto one row of Table A;Table 430 Compounds of formula I.B18 (I.B18-20.1-I.B18-20.2304) in whichB is N, R² is 3-methyl-isoxazolin-5-yl, R⁴ is CH₃ and R⁵ is Cl and thecombination of R¹, R³, R⁶ and R⁷ for a compound corresponds in each caseto one row of Table A;Table 431 Compounds of formula I.B19 (I.B19-11.1-I.B19-11.2304) in whichB is N, R² is 3-methyl-isoxazol-5-yl, R⁴ is H and R⁵ is F and thecombination of R¹, R³, R⁶ and R⁷ for a compound corresponds in each caseto one row of Table A;Table 432 Compounds of formula I.B19 (I.B19-12.1-I.B19-12.2304) in whichB is N, R² is 3-methyl-isoxazol-5-yl, R⁴ is H and R⁵ is Cl and thecombination of R¹, R³, R⁶ and R⁷ for a compound corresponds in each caseto one row of Table A;Table 433 Compounds of formula I.B19 (I.B19-13.1-I.B19-13.2304) in whichB is N, R² is 3-methyl-isoxazol-5-yl, R⁴ is F and R⁵ is F and thecombination of R¹, R³, R⁶ and R⁷ for a compound corresponds in each caseto one row of Table A;Table 434 Compounds of formula I.B19 (I.B19-14.1-I.B19-14.2304) in whichB is N, R² is 3-methyl-isoxazol-5-yl, R⁴ is F and R⁵ is Cl and thecombination of R¹, R³, R⁶ and R⁷ for a compound corresponds in each caseto one row of Table A;Table 435 Compounds of formula I.B19 (I.B19-15.1-I.B19-15.2304) in whichB is N, R² is 3-methyl-isoxazol-5-yl, R⁴ is Cl and R⁵ is F and thecombination of R¹, R³, R⁶ and R⁷ for a compound corresponds in each caseto one row of Table A;Table 436 Compounds of formula I.B19 (I.B19-16.1-I.B19-16.2304) in whichB is N, R² is 3-methyl-isoxazol-5-yl, R⁴ is Cl and R⁵ is Cl and thecombination of R¹, R³, R⁶ and R⁷ for a compound corresponds in each caseto one row of Table A;Table 437 Compounds of formula I.B19 (I.B19-17.1-I.B19-17.2304) in whichB is N, R² is 3-methyl-isoxazol-5-yl, R⁴ is CN and R⁵ is F and thecombination of R¹, R³, R⁶ and R⁷ for a compound corresponds in each caseto one row of Table A;Table 438 Compounds of formula I.B19 (I.B19-18.1-I.B19-18.2304) in whichB is N, R² is 3-methyl-isoxazol-5-yl, R⁴ is CN and R⁵ is Cl and thecombination of R¹, R³, R⁶ and R⁷ for a compound corresponds in each caseto one row of Table A;Table 439 Compounds of formula I.B19 (I.B19-19.1-I.B19-19.2304) in whichB is N, R² is 3-methyl-isoxazol-5-yl, R⁴ is CH₃ and R⁵ is F and thecombination of R¹, R³, R⁶ and R⁷ for a compound corresponds in each caseto one row of Table A;Table 440 Compounds of formula I.B19 (I.B19-20.1-I.B19-20.2304) in whichB is N, R² is 3-methyl-isoxazol-5-yl, R⁴ is CH₃ and R⁵ is Cl and thecombination of R¹, R³, R⁶ and R⁷ for a compound corresponds in each caseto one row of Table A;Table 441 Compounds of formula I.B20 (I.B20-11.1-I.B20-11.2304) in whichB is N, R² is CH₃, R⁴ is H and R⁵ is F and the combination of R¹, R³, R⁶and R⁷ for a compound corresponds in each case to one row of Table A;Table 442 Compounds of formula I.B20 (I.B20-12.1-I.B20-12.2304) in whichB is N, R² is CH₃, R⁴ is H and R⁵ is Cl and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 443 Compounds of formula I.B20 (I.B20-13.1-I.B20-13.2304) in whichB is N, R² is CH₃, R⁴ is F and R⁵ is F and the combination of R¹, R³, R⁶and R⁷ for a compound corresponds in each case to one row of Table A;Table 444 Compounds of formula I.B20 (I.B20-14.1-I.B20-14.2304) in whichB is N, R² is CH₃, R⁴ is F and R⁵ is Cl and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 445 Compounds of formula I.B20 (I.B20-15.1-I.B20-15.2304) in whichB is N, R² is CH₃, R⁴ is Cl and R⁵ is F and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 446 Compounds of formula I.B20 (I.B20-16.1-I.B20-16.2304) in whichB is N, R² is CH₃, R⁴ is Cl and R⁵ is Cl and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 447 Compounds of formula I.B20 (I.B20-17.1-I.B20-17.2304) in whichB is N, R² is CH₃, R⁴ is CN and R⁵ is F and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 448 Compounds of formula I.B20 (I.B20-18.1-I.B20-18.2304) in whichB is N, R² is CH₃, R⁴ is CN and R⁵ is Cl and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 449 Compounds of formula I.B20 (I.B20-19.1-I.B20-19.2304) in whichB is N, R² is CH₃, R⁴ is CH₃ and R⁵ is F and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 450 Compounds of formula I.B20 (I.B20-20.1-I.B20-20.2304) in whichB is N, R² is CH₃, R⁴ is CH₃ and R⁵ is Cl and the combination of R¹, R³,R⁶ and R⁷ for a compound corresponds in each case to one row of Table A;Table 451 Compounds of formula I.B21 (I.B21-11.1-I.B21-11.2304) in whichB is N, R² is CH₂OCH₃, R⁴ is H and R⁵ is F and the combination of R¹,R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 452 Compounds of formula I.B21 (I.B21-12.1-I.B21-12.2304) in whichB is N, R² is CH₂OCH₃, R⁴ is H and R⁵ is Cl and the combination of R¹,R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 453 Compounds of formula I.B21 (I.B21-13.1-I.B21-13.2304) in whichB is N, R² is CH₂OCH₃, R⁴ is F and R⁵ is F and the combination of R¹,R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 454 Compounds of formula I.B21 (I.B21-14.1-I.B21-14.2304) in whichB is N, R² is CH₂OCH₃, R⁴ is F and R⁵ is Cl and the combination of R¹,R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 455 Compounds of formula I.B21 (I.B21-15.1-I.B21-15.2304) in whichB is N, R² is CH₂OCH₃, R⁴ is Cl and R⁵ is F and the combination of R¹,R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 456 Compounds of formula I.B21 (I.B21-16.1-I.B21-16.2304) in whichB is N, R² is CH₂OCH₃, R⁴ is Cl and R⁵ is Cl and the combination of R¹,R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 457 Compounds of formula I.B21 (I.B21-17.1-I.B21-17.2304) in whichB is N, R² is CH₂OCH₃, R⁴ is CN and R⁵ is F and the combination of R¹,R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 458 Compounds of formula I.B21 (I.B21-18.1-I.B21-18.2304) in whichB is N, R² is CH₂OCH₃, R⁴ is CN and R⁵ is Cl and the combination of R¹,R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 459 Compounds of formula I.B21 (I.B21-19.1-I.B21-19.2304) in whichB is N, R² is CH₂OCH₃, R⁴ is CH₃ and R⁵ is F and the combination of R¹,R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 460 Compounds of formula I.B21 (I.B21-20.1-I.B21-20.2304) in whichB is N, R² is CH₂OCH₃, R⁴ is CH₃ and R⁵ is Cl and the combination of R¹,R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 461 Compounds of formula I.B22 (I.B22-11.1-I.B22-11.2304) in whichB is N, R² is OCH₂CH(CH₂)₂, R⁴ is H and R⁵ is F and the combination ofR¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 462 Compounds of formula I.B22 (I.B22-12.1-I.B22-12.2304) in whichB is N, R² is OCH₂CH(CH₂)₂, R⁴ is H and R⁵ is Cl and the combination ofR¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 463 Compounds of formula I.B22 (I.B22-13.1-I.B22-13.2304) in whichB is N, R² is OCH₂CH(CH₂)₂, R⁴ is F and R⁵ is F and the combination ofR¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 464 Compounds of formula I.B22 (I.B22-14.1-I.B22-14.2304) in whichB is N, R² is OCH₂CH(CH₂)₂, R⁴ is F and R⁵ is Cl and the combination ofR¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 465 Compounds of formula I.B22 (I.B22-15.1-I.B22-15.2304) in whichB is N, R² is OCH₂CH(CH₂)₂, R⁴ is Cl and R⁵ is F and the combination ofR¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 466 Compounds of formula I.B22 (I.B22-16.1-I.B22-16.2304) in whichB is N, R² is OCH₂CH(CH₂)₂, R⁴ is Cl and R⁵ is Cl and the combination ofR¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 467 Compounds of formula I.B22 (I.B22-17.1-I.B22-17.2304) in whichB is N, R² is OCH₂CH(CH₂)₂, R⁴ is CN and R⁵ is F and the combination ofR¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 468 Compounds of formula I.B22 (I.B22-18.1-I.B22-18.2304) in whichB is N, R² is OCH₂CH(CH₂)₂, R⁴ is CN and R⁵ is Cl and the combination ofR¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 469 Compounds of formula I.B22 (I.B22-19.1-I.B22-19.2304) in whichB is N, R² is OCH₂CH(CH₂)₂, R⁴ is CH₃ and R⁵ is F and the combination ofR¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 470 Compounds of formula I.B22 (I.B22-20.1-I.B22-20.2304) in whichB is N, R² is OCH₂CH(CH₂)₂, R⁴ is CH₃ and R⁵ is Cl and the combinationof R¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one rowof Table A;Table 471 Compounds of formula I.B23 (I.B23-11.1-I.B23-11.2304) in whichB is N, R² is NCH₃SO₂CH₃, R⁴ is H and R⁵ is F and the combination of R¹,R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 472 Compounds of formula I.B23 (I.B23-12.1-I.B23-12.2304) in whichB is N, R² is NCH₃SO₂CH₃, R⁴ is H and R⁵ is Cl and the combination ofR¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 473 Compounds of formula I.B23 (I.B23-13.1-I.B23-13.2304) in whichB is N, R² is NCH₃SO₂CH₃, R⁴ is F and R⁵ is F and the combination of R¹,R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 474 Compounds of formula I.B23 (I.B23-14.1-I.B23-14.2304) in whichB is N, R² is NCH₃SO₂CH₃, R⁴ is F and R⁵ is Cl and the combination ofR¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 475 Compounds of formula I.B23 (I.B23-15.1-I.B23-15.2304) in whichB is N, R² is NCH₃SO₂CH₃, R⁴ is Cl and R⁵ is F and the combination ofR¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 476 Compounds of formula I.B23 (I.B23-16.1-I.B23-16.2304) in whichB is N, R² is NCH₃SO₂CH₃, R⁴ is Cl and R⁵ is Cl and the combination ofR¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 477 Compounds of formula I.B23 (I.B23-17.1-I.B23-17.2304) in whichB is N, R² is NCH₃SO₂CH₃, R⁴ is CN and R⁵ is F and the combination ofR¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 478 Compounds of formula I.B23 (I.B23-18.1-I.B23-18.2304) in whichB is N, R² is NCH₃SO₂CH₃, R⁴ is CN and R⁵ is Cl and the combination ofR¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 479 Compounds of formula I.B23 (I.B23-19.1-I.B23-19.2304) in whichB is N, R² is NCH₃SO₂CH₃, R⁴ is CH₃ and R⁵ is F and the combination ofR¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;Table 480 Compounds of formula I.B23 (I.B23-20.1-I.B23-20.2304) in whichB is N, R² is NCH₃SO₂CH₃, R⁴ is CH₃ and R⁵ is Cl and the combination ofR¹, R³, R⁶ and R⁷ for a compound corresponds in each case to one row ofTable A;

The compounds of formula I can be prepared by standard methods oforganic chemistry, e.g. by the methods described hereinafter in schemes1 to 8. The substituents, variables and indices in schemes 1 to 8 are asdefined above for formula I, if not otherwise specified.

The compounds of formula I can be prepared analogous to Scheme 1 below.

5-Amino-1-R-1,2,4-triazole or 5-amino-1-R-tetrazole compounds of formulaIII can be re-acted with benzoyl derivatives of formula II to affordcompounds of formula I. X is a leaving group, such as halogen, inparticular Cl, an anhydride residue or an active ester residue.Especially in case of X being halogen the reaction is suitably carriedout in the presence of a base. Suitable bases are for examplecarbonates, such as lithium, sodium or potassium carbonates, amines,such as trimethylamine or triethylamine, and basic N-heterocycles, suchas pyridine, 2,6-dimethylpyridine or 2,4,6-trimethylpyridine. Suitablesolvents are in particular aprotic solvents such as pentane, hexane,heptane, octane, cyclohexane, dichloromethane, chloroform,1,2-dichlorethane, benzene, chlorobenzene, toluene, the xylenes,dichlorobenzene, trimethylbenzene, pyridine, 2,6-dimethylpyridine,2,4,6-trimethylpyridine, acetonitrile, diethyl ether, tetrahydrofuran,2-methyl tetrahydrofuran, methyl tert-butylether, 1,4-dioxane,N,N-dimethyl formamide, N-methyl pyrrolidinone or mixtures thereof. Thestarting materials are generally re-acted with one another in equimolaror nearly equimolar amounts at a reaction temperature usually in therange of −20° C. to 100° C. and preferably in the range of −5° C. to 50°C.

Alternatively, compounds of formula I can also be prepared as shown inScheme 2. Reaction of 5-amino-1-R-1,2,4-triazole or5-amino-1-R-tetrazole of formula III with a benzoic acid derivative offormula IV yields compound I. The reaction is preferably carried out inthe presence of a suitable activating agent, which converts the acidgroup of compound IV into an activated ester or amide. For this purposeactivating agents known in the art, such as 1,1′,carbonyldiimidazole(CDI), dicyclohexyl carbodiimide (DCC),1-ethyl-3-(3-dimethylaminopropyl)carbodiimide (EDC) or2,4,6-tripropyl-1,3,5,2,4,6-trioxatriphosphorinane-2,4,6-trioxide (T3P)can be employed. The activated ester or amide can be formed, dependingin particular on the specific activating agent used, either in situ bycontacting compound IV with the activating agent in the presence ofcompound III, or in a separate step prior to the reaction with compoundIII. It may be advantageous, especially in cases where DCC or EDC areused as activating agent, to include further additives in the activatingreaction, such as hydroxybenzotriazole (HOBt), nitrophenol,pentafluorophenol, 2,4,5-trichlorophenol or N-hydroxysuccinimide. It mayfurther be advantageous to prepare the activated ester or amide in thepresence of a base, for example a tertiary amine. The activated ester oramide is either in situ or subsequently re-acted with the amine offormula III to afford the amide of formula I. The reaction normallytakes place in anhydrous inert solvents, such as chlorinatedhydrocarbons, e.g. dichloromethane or dichloroethane, ethers, e.g.tetrahydrofuran or 1,4-dioxane or carboxamides, e.g.N,N-dimethylformamide, N,N-dimethylacetamide or N-methylpyrrolidone. Thereaction is ordinarily carried out at temperatures in the range from−20° C. to +25° C.

The compounds of formula II and their respective benzoic acid precursorsof formula IV can be purchased or can be prepared by processes known inthe art or disclosed in the literature, e.g. in WO 9746530, WO 9831676,WO 9831681, WO 2002/018352, WO 2000/003988, US 2007/0191335, U.S. Pat.No. 6,277,847.

Furthermore, compounds of formula I, can be obtained by treatingN-(1H-1,2,4-triazol-5-yl)benzamides or N-(1H-tetrazol-5-yl)benzamides offormula V with, for example, alkylating agents such as alkyl halidesaccording to Scheme 3.

The 5-amino-1-R-tetrazoles of formula III, where R is for example alkyl,are either commercially available or are obtainable according to methodsknown from the literature. For example, 5-amino-1-R-tetrazole can beprepared from 5-aminotetrazole according to the method described in theJournal of the American Chemical Society, 1954, 76, 923-924 (Scheme 4).

Alternatively, 5-amino-1-R-tetrazole compounds of formula III can beprepared according to the method described in the Journal of theAmerican Chemical Society, 1954, 76, 88-89 (Scheme 5).

As shown in Scheme 6, 5-amino-1-R-triazoles of formula III, where R isfor example alkyl, are either commercially available or are obtainableaccording to methods described in the literature. For example,5-amino-1-R-triazole can be prepared from 5-aminotriazole according tothe method described in Zeitschrift fuir Chemie, 1990, 30, 12, 436-437.

5-Amino-1-R-triazole compounds of formula III, can also be preparedanalogous to the synthesis described in Chemische Berichte, 1964, 97, 2,396-404, as shown in Scheme 7.

As a rule, the compounds of formula I including their stereoisomers,salts, tautomers and N-oxides, and their precursors in the synthesisprocess, can be prepared by the methods described above. If individualcompounds can not be prepared via the above-described routes, they canbe prepared by derivatization of other compounds I or the respectiveprecursor or by customary modifications of the synthesis routesdescribed. For example, in individual cases, certain compounds offormula I can advantageously be prepared from other compounds of formulaI by derivatization, e.g. by ester hydrolysis, amidation,esterification, ether cleavage, olefination, reduction, oxidation andthe like, or by customary modifications of the synthesis routesdescribed.

The reaction mixtures are worked up in the customary manner, for exampleby mixing with water, separating the phases, and, if appropriate,purifying the crude products by chromatography, for example on aluminaor on silica gel. Some of the intermediates and end products may beobtained in the form of colorless or pale brown viscous oils which arefreed or purified from volatile components under reduced pressure and atmoderately elevated temperature. If the intermediates and end productsare obtained as solids, they may be purified by recrystallization ortrituration.

The compounds of formula I and their agriculturally suitable salts areuseful as herbicides. They are useful as such or as an appropriatelyformulated composition. The herbicidal compositions comprising thecompound I, in particular the preferred aspects thereof, controlvegetation on non-crop areas very efficiently, especially at high ratesof application. They act against broad-leaved weeds and weed grasses incrops such as wheat, rice, corn, soybeans and cotton without causing anysignificant damage to the crop plants. This effect is mainly observed atlow rates of application.

Depending on the application method in question, the compounds offormula I, in particular the preferred aspects thereof, or compositionscomprising them can additionally be employed in a further number of cropplants for eliminating unwanted plants. Examples of suitable crops arethe following:

Allium cepa, Ananas comosus, Arachis hypogaea, Asparagus officinalis,Avena sativa, Beta vulgaris spec. altissima, Beta vulgaris spec. rapa,Brassica napus var. napus, Brassica napus var. napobrassica, Brassicarapa var. silvestris, Brassica oleracea, Brassica nigra, Camelliasinensis, Carthamus tinctorius, Carya illinoinensis, Citrus limon,Citrus sinensis, Coffea arabica (Coffea canephora, Coffea liberica),Cucumis sativus, Cynodon dactylon, Daucus carota, Elaeis guineensis,Fragaria vesca, Glycine max, Gossypium hirsutum, (Gossypium arboreum,Gossypium herbaceum, Gossypium vitifolium), Helianthus annuus, Heveabrasiliensis, Hordeum vulgare, Humulus lupulus, Ipomoea batatas, Juglansregia, Lens culinaris, Linum usitatissimum, Lycopersicon lycopersicum,Malus spec., Manihot esculenta, Medicago sativa, Musa spec., Nicotianatabacum (N. rustica), Olea europaea, Oryza sativa, Phaseolus lunatus,Phaseolus vulgaris, Picea abies, Pinus spec., Pistacia vera, Pisumsativum, Prunus avium, Prunus persica, Pyrus communis, Prunus armeniaca,Prunus cerasus, Prunus dulcis and Prunus domestica, Ribes sylvestre,Ricinus communis, Saccharum officinarum, Secale cereale, Sinapis alba,Solanum tuberosum, Sorghum bicolor (s. vulgare), Theobroma cacao,Trifolium pratense, Triticum aestivum, Triticale, Triticum durum, Viciafaba, Vitis vinifera, Zea mays.

The term “crop plants” also includes plants which have been modified bybreeding, muta-genesis or genetic engineering. Genetically modifiedplants are plants whose genetic material has been modified in a mannerwhich does not occur under natural conditions by crossing, mutations ornatural recombination (i.e. reassembly of the genetic information).Here, in general, one or more genes are integrated into the geneticmaterial of the plant to improve the properties of the plant.

Accordingly, the term “crop plants” also includes plants which, bybreeding and genetic engineering, have acquired tolerance to certainclasses of herbicides, such as hydroxy-phenylpyruvate dioxygenase (HPPD)inhibitors, acetolactate synthase (ALS) inhibitors, such as, forexample, sulfonylureas (EP-A-0257993, U.S. Pat. No. 5,013,659) orimidazolinones (see, for example, U.S. Pat. No. 6,222,100, WO 01/82685,WO 00/26390, WO 97/41218, WO 98/02526, WO 98/02527, WO 04/106529, WO05/20673, WO 03/14357, WO 03/13225, WO 03/14356, WO 04/16073),enolpyruvylshikimate 3-phosphate synthase (EPSPS) inhibitors, such as,for example, glyphosate (see, for example, WO 92/00377), glutaminesynthetase (GS) inhibitors, such as, for example, glufosinate (see, forexample, EP-A-0242236, EP-A-242246), or oxynil herbicides (see, forexample, U.S. Pat. No. 5,559,024).

Numerous crop plants, for example Clearfield® oilseed rape, tolerant toimidazolinones, for example imazamox, have been generated with the aidof classic breeding methods (muta-genesis). Crop plants such assoybeans, cotton, corn, beet and oilseed rape, resistant to glyphosateor glufosinate, which are available under the tradenames RoundupReady®(glyphosate) and Liberty Link® (glufosinate) have been generated withthe aid of genetic engineering methods.

Accordingly, the term “crop plants” also includes plants which, with theaid of genetic engineering, produce one or more toxins, for examplethose of the bacterial strain Bacillus ssp. Toxins which are produced bysuch genetically modified plants include, for example, insecticidalproteins of Bacillus spp., in particular B. thuringiensis, such as theendotoxins Cry1Ab, Cry1Ac, Cry1F, Cry1Fa2, Cry2Ab, Cry3A, Cry3Bb1,Cry9c, Cry34Ab1 or Cry35Ab1; or vegetative insecticidal proteins (VIPs),for example VIP1, VIP2, VIP3, or VIP3A; insecticidal proteins ofnema-tode-colonizing bacteria, for example Photorhabdus spp. orXenorhabdus spp.; toxins of animal organisms, for example wasp, spideror scorpion toxins; fungal toxins, for example from Streptomycetes;plant lectins, for example from peas or barley; agglutinins; proteinaseinhibitors, for example trypsin inhibitors, serine protease inhibitors,patatin, cystatin or papain inhibitors, ribo-some-inactivating proteins(RIPs), for example ricin, corn-RIP, abrin, luffin, saporin or bryodin;steroid-metabolizing enzymes, for example 3-hydroxysteroid oxidase,ecdysteroid-IDP glycosyl transferase, cholesterol oxidase, ecdysoneinhibitors, or HMG-CoA reductase; ion channel blockers, for exampleinhibitors of sodium channels or calcium channels; juvenile hormonees-terase; receptors of the diuretic hormone (helicokinin receptors);stilbene synthase, bibenzyl synthase, chitinases and glucanases. In theplants, these toxins may also be produced as pre-toxins, hybrid proteinsor truncated or otherwise modified proteins. Hybrid proteins arecharac-terized by a novel combination of different protein domains (see,for example, WO 2002/015701). Further examples of such toxins orgenetically modified plants which produce these toxins are disclosed inEP-A 374 753, WO 93/007278, WO 95/34656, EP-A 427 529, EP-A 451 878, WO03/018810 and WO 03/052073. The methods for producing these geneticallymodified plants are known to the person skilled in the art anddisclosed, for example, in the publications mentioned above. Numerous ofthe toxins mentioned above bestow, upon the plants by which they areproduced, tolerance to pests from all taxonomic classes of arthropods,in particular to beetles (Coeleropta), dipterans (Diptera) andbutterflies (Lepidoptera) and to nema-todes (Nematoda).

Genetically modified plants which produce one or more genes coding forinsecticidal toxins are described, for example, in the publicationsmentioned above, and some of them are commercially available, such as,for example, YieldGard® (corn varieties producing the toxin Cry1Ab),YieldGard® Plus (corn varieties which produce the toxins Cry1Ab andCry3Bb1), Star-link® (corn varieties which produce the toxin Cry9c),Herculex® RW (corn varieties which produce the toxins Cry34Ab1, Cry35Ab1and the enzyme phosphinothricin-N-acetyltransferase [PAT]); NuCOTN® 33B(cotton varieties which produce the toxin Cry1Ac), Bollgard® I (cottonvarieties which produce the toxin Cry1Ac), Bollgard® II (cottonvarieties which produce the toxins Cry1Ac and Cry2Ab2); VIPCOT® (cottonvarieties which produce a VIP toxin); NewLeaf® (potato varieties whichproduce the toxin Cry3A); Bt-Xtra®, NatureGard®, KnockOut®, BiteGard®,Protecta®, Btl 1 (for example Agrisure® CB) and Bt176 from SyngentaSeeds SAS, France (corn varieties which produce the toxin Cry1Ab and thePAT enyzme), MIR604 from Syngenta Seeds SAS, France (corn varietieswhich produce a modified version of the toxin Cry3A, see WO 03/018810),MON 863 from Monsanto Europe S.A., Belgium (corn varieties which producethe toxin Cry3Bb1), IPC 531 from Monsanto Europe S.A., Belgium (cottonvarieties which produce a modified version of the toxin Cry1Ac) and 1507from Pioneer Overseas Corporation, Belgium (corn varieties which producethe toxin Cry1F and the PAT enzyme).

Accordingly, the term “crop plants” also includes plants which, with theaid of genetic engineering, produce one or more proteins which are morerobust or have increased resistance to bacterial, viral or fungalpathogens, such as, for example, pathogenesis-related proteins (PRproteins, see EP-A 0 392 225), resistance proteins (for example potatovarieties producing two resistance genes against Phytophthora infestansfrom the wild Mexican potato Solanum bulbocastanum) or T4 lysozyme (forexample potato cultivars which, by producing this protein, are resistantto bacteria such as Erwinia amylvora).

Accordingly, the term “crop plants” also includes plants whoseproductivity has been improved with the aid of genetic engineeringmethods, for example by enhancing the potential yield (for examplebiomass, grain yield, starch, oil or protein content), tolerance todrought, salt or other limiting environmental factors or resistance topests and fungal, bacterial and viral pathogens.

The term “crop plants” also includes plants whose ingredients have beenmodified with the aid of genetic engineering methods in particular forimproving human or animal diet, for example by oil plants producinghealth-promoting long-chain omega 3 fatty acids or monounsaturated omega9 fatty acids (for example Nexera® oilseed rape).

The term “crop plants” also includes plants which have been modifiedwith the aid of genetic engineering methods for improving the productionof raw materials, for example by increasing the amylopectin content ofpotatoes (Amflora® potato).

Furthermore, it has been found that the compounds of formula I are alsosuitable for the defoliation and/or desiccation of plant parts, forwhich crop plants such as cotton, potato, oilseed rape, sunflower,soybean or field beans, in particular cotton, are suitable. In thisregard, there have been found compositions for the desiccation and/ordefoliation of plants, processes for preparing these compositions andmethods for desiccating and/or defoliating plants using the compounds offormula I.

As desiccants, the compounds of formula I are particularly suitable fordesiccating the above-ground parts of crop plants such as potato,oilseed rape, sunflower and soybean, but also cereals. This makespossible the fully mechanical harvesting of these important crop plants.

Also of economic interest is to facilitate harvesting, which is madepossible by concentrating within a certain period of time thedehiscence, or reduction of adhesion to the tree, in citrus fruit,olives and other species and varieties of pomaceous fruit, stone fruitand nuts. The same mechanism, i.e. the promotion of the development ofabscission tissue between fruit part or leaf part and shoot part of theplants is also essential for the readily controllable defoliation ofuseful plants, in particular cotton.

Moreover, a shortening of the time interval in which the individualcotton plants mature leads to an increased fiber quality afterharvesting.

The compounds of formula I, or the herbicidal compositions comprisingthe compounds of formula I, can be used, for example, in the form ofready-to-spray aqueous solutions, powders, suspensions, also highlyconcentrated aqueous, oily or other suspensions or dispersions,emulsions, oil dispersions, pastes, dusts, materials for broadcasting,or granules, by means of spraying, atomizing, dusting, spreading,watering or treatment of the seed or mixing with the seed. The use formsdepend on the intended purpose; in each case, they should ensure thefinest possible distribution of the active ingredients according to theinvention.

The herbicidal compositions comprise a herbicidally effective amount ofat least one compound of the formula I or an agriculturally useful saltof I, and auxiliaries which are customary for the formulation of cropprotection agents.

Examples of auxiliaries customary for the formulation of crop protectionagents are inert auxiliaries, solid carriers, surfactants (such asdispersants, protective colloids, emulsifiers, wetting agents andtackifiers), organic and inorganic thickeners, bactericides, antifreezeagents, antifoams, if appropriate colorants and, for seed formulations,adhesives.

Examples of thickeners (i.e. compounds which impart to the formulationmodified flow properties, i.e. high viscosity in the state of rest andlow viscosity in motion) are polysaccharides, such as xanthan gum(Kelzan® from Kelco), Rhodopol® 23 (Rhone Poulenc) or Veegum® (from R.T.Vanderbilt), and also organic and inorganic sheet minerals, such asAttaclay® (from Engelhardt).

Examples of antifoams are silicone emulsions (such as, for example,Silikon® SRE, Wacker or Rhodorsil® from Rhodia), long-chain alcohols,fatty acids, salts of fatty acids, organofluorine compounds and mixturesthereof.

Bactericides can be added for stabilizing the aqueous herbicidalformulation. Examples of bactericides are bactericides based ondiclorophen and benzyl alcohol hemiformal (Proxel® from ICI or Acticide®RS from Thor Chemie and Kathon® MK from Rohm & Haas), and alsoisothiazolinone derivates, such as alkylisothiazolinones andbenzisothiazolinones (Acticide MBS from Thor Chemie).

Examples of antifreeze agents are ethylene glycol, propylene glycol,urea or glycerol.

Examples of colorants are both sparingly water-soluble pigments andwater-soluble dyes. Examples which may be mentioned are the dyes knownunder the names Rhodamin B, C.I. Pigment Red 112 and C.I. Solvent Red 1,and also pigment blue 15:4, pigment blue 15:3, pigment blue 15:2,pigment blue 15:1, pigment blue 80, pigment yellow 1, pigment yellow 13,pigment red 112, pigment red 48:2, pigment red 48:1, pigment red 57:1,pigment red 53:1, pigment orange 43, pigment orange 34, pigment orange5, pigment green 36, pigment green 7, pigment white 6, pigment brown 25,basic violet 10, basic violet 49, acid red 51, acid red 52, acid red 14,acid blue 9, acid yellow 23, basic red 10, basic red 108.

Examples of adhesives are polyvinylpyrrolidone, polyvinyl acetate,polyvinyl alcohol and tylose.

Suitable inert auxiliaries are, for example, the following:

mineral oil fractions of medium to high boiling point, such as keroseneand diesel oil, furthermore coal tar oils and oils of vegetable oranimal origin, aliphatic, cyclic and aromatic hydrocarbons, for exampleparaffin, tetrahydronaphthalene, alkylated naphthalenes and theirderivatives, alkylated benzenes and their derivatives, alcohols such asmethanol, ethanol, propanol, butanol and cyclohexanol, ketones such ascyclohexanone or strongly polar solvents, for example amines such asN-methylpyrrolidone, and water.

Solid carriers are mineral earths such as silicas, silica gels,silicates, talc, kaolin, limestone, lime, chalk, bole, loess, clay,dolomite, diatomaceous earth, calcium sulfate, magnesium sulfate andmagnesium oxide, ground synthetic materials, fertilizers such asammonium sulfate, ammonium phosphate, ammonium nitrate and ureas, andproducts of vegetable origin, such as cereal meal, tree bark meal, woodmeal and nutshell meal, cellulose powders, or other solid carriers.

Suitable surfactants (adjuvants, wetting agents, tackifiers, dispersantsand also emulsifiers) are the alkali metal salts, alkaline earth metalsalts and ammonium salts of aromatic sulfonic acids, for examplelignosulfonic acids (e.g. Borrespers-types, Borregaard), phenolsulfonicacids, naphthalenesulfonic acids (Morwet types, Akzo Nobel) anddibutylnaphthalenesulfonic acid (Nekal types, BASF SE), and of fattyacids, alkyl- and alkylarylsulfonates, alkyl sulfates, lauryl ethersulfates and fatty alcohol sulfates, and salts of sulfated hexa-, hepta-and octadecanols, and also of fatty alcohol glycol ethers, condensatesof sulfonated naphthalene and its derivatives with formaldehyde,condensates of naphthalene or of the naphthalenesulfonic acids withphenol and formaldehyde, polyoxyethylene octylphenol ether, ethoxylatedisooctyl-, octyl- or nonylphenol, alkylphenyl or tributylphenylpolyglycol ether, alkylaryl polyether alcohols, isotridecyl alcohol,fatty alcohol/ethylene oxide condensates, ethoxylated castor oil,polyoxyethylene alkyl ethers or polyoxypropylene alkyl ethers, laurylalcohol polyglycol ether acetate, sorbitol esters, lignosulfite wasteliquors and proteins, denatured proteins, polysaccharides (e.g.methylcellulose), hydrophobically modified starches, polyvinyl alcohol(Mowiol types Clariant), polycarboxylates (BASF SE, Sokalan types),polyalkoxylates, polyvinylamine (BASF SE, Lupamine types),polyethyleneimine (BASF SE, Lupasol types), polyvinylpyrrolidone andcopolymers thereof.

Powders, materials for broadcasting and dusts can be prepared by mixingor grinding the active ingredients together with a solid carrier.

Granules, for example coated granules, impregnated granules andhomogeneous granules, can be prepared by binding the active ingredientsto solid carriers.

Aqueous use forms can be prepared from emulsion concentrates,suspensions, pastes, wettable powders or water-dispersible granules byadding water. To prepare emulsions, pastes or oil dispersions, thecompounds of formula I or Ia, either as such or dissolved in an oil orsolvent, can be homogenized in water by means of a wetting agent,tackifier, dispersant or emulsifier. Alternatively, it is also possibleto prepare concentrates comprising active substance, wetting agent,tackifier, dispersant or emulsifier and, if desired, solvent or oil,which are suitable for dilution with water.

The concentrations of the compounds of formula I in the ready-to-usepreparations can be varied within wide ranges. In general, theformulations comprise from 0.001 to 98% by weight, preferably 0.01 to95% by weight of at least one active compound. The active compounds areemployed in a purity of from 90% to 100%, preferably 95% to 100%(according to NMR spectrum).

The formulations or ready-to-use preparations may also comprise acids,bases or buffer systems, suitable examples being phosphoric acid orsulfuric acid, or urea or ammonia.

The compounds of formula I of the invention can for example beformulated as follows:

1. Products for Dilution with Water

A. Water-Soluble Concentrates

parts by weight of active compound are dissolved in 90 parts by weightof water or a water-soluble solvent. As an alternative, wetters or otheradjuvants are added. The active compound dissolves upon dilution withwater. This gives a formulation with an active compound content of 10%by weight.

B. Dispersible Concentrates

parts by weight of active compound are dissolved in 70 parts by weightof cyclohexanone with addition of 10 parts by weight of a dispersant,for example polyvinylpyrrolidone. Dilution with water gives adispersion. The active compound content is 20% by weight.

C. Emulsifiable Concentrates

parts by weight of active compound are dissolved in 75 parts by weightof an organic solvent (e.g. alkylaromatics) with addition of calciumdodecylbenzenesulfonate and castor oil ethoxylate (in each case 5 partsby weight). Dilution with water gives an emulsion. The formulation hasan active compound content of 15% by weight.

D. Emulsions

parts by weight of active compound are dissolved in 35 parts by weightof an organic solvent (e.g. alkylaromatics) with addition of calciumdodecylbenzenesulfonate and castor oil ethoxylate (in each case 5 partsby weight). This mixture is introduced into 30 parts by weight of waterby means of an emulsifier (e.g. Ultraturrax) and made into a homogeneousemulsion. Dilution with water gives an emulsion. The formulation has anactive compound content of 25% by weight.

E. Suspensions

In an agitated ball mill, 20 parts by weight of active compound arecomminuted with addition of 10 parts by weight of dispersants andwetters and 70 parts by weight of water or an organic solvent to give afine active compound suspension. Dilution with water gives a stablesuspension of the active compound. The active compound content in theformulation is 20% by weight.

F. Water-Dispersible Granules and Water-Soluble Granules

50 parts by weight of active compound are ground finely with addition of50 parts by weight of dispersants and wetters and made intowater-dispersible or water-soluble granules by means of technicalappliances (for example extrusion, spray tower, fluidized bed). Dilutionwith water gives a stable dispersion or solution of the active compound.The formulation has an active compound content of 50% by weight.

G. Water-Dispersible Powders and Water-Soluble Powders

75 parts by weight of active compound are ground in a rotor-stator millwith addition of 25 parts by weight of dispersants, wetters and silicagel. Dilution with water gives a stable dispersion or solution of theactive compound. The active compound content of the formulation is 75%by weight.

H. Gel Formulations

In a ball mill, 20 parts by weight of active compound, 10 parts byweight of dispersant, 1 part by weight of gelling agent and 70 parts byweight of water or of an organic solvent are ground to give a finesuspension. Dilution with water gives a stable suspension with activecompound content of 20% by weight.

2. Products to be Applied Undiluted

I. Dusts

5 parts by weight of active compound are ground finely and mixedintimately with 95 parts by weight of finely divided kaolin. This givesa dusting powder with an active compound content of 5% by weight.

J. Granules (GR, FG, GG, MG)

0.5 parts by weight of active compound are ground finely and associatedwith 99.5 parts by weight of carriers. Current methods here areextrusion, spray-drying or the fluidized bed.

This gives granules to be applied undiluted with an active compoundcontent of 0.5% by weight.

K. ULV Solutions (UL)

10 parts by weight of active compound are dissolved in 90 parts byweight of an organic solvent, for example xylene. This gives a productto be applied undiluted with an active compound content of 10% byweight.

The compounds of formula I or the herbicidal compositions comprisingthem can be applied pre- or post-emergence, or together with the seed ofa crop plant. It is also possible to apply the herbicidal compositionsor active compounds by applying seed, pretreated with the herbicidalcompositions or active compounds, of a crop plant. If the activecompounds are less well tolerated by certain crop plants, applicationtechniques may be used in which the herbicidal compositions are sprayed,with the aid of the spraying equipment, in such a way that as far aspossible they do not come into contact with the leaves of the sensitivecrop plants, while the active compounds reach the leaves of undesirableplants growing underneath, or the bare soil surface (post-directed,lay-by).

In a further embodiment, the compounds of formula I or the herbicidalcompositions can be applied by treating seed.

The treatment of seed comprises essentially all procedures familiar tothe person skilled in the art (seed dressing, seed coating, seeddusting, seed soaking, seed film coating, seed multi-layer coating, seedencrusting, seed dripping and seed pelleting) based on the compounds offormula I according to the invention or the compositions preparedtherefrom. Here, the herbicidal compositions can be applied diluted orundiluted.

The term seed comprises seed of all types, such as, for example, corns,seeds, fruits, tubers, cuttings and similar forms. Here, preferably, theterm seed describes corns and seeds.

The seed used can be seed of the useful plants mentioned above, but alsothe seed of transgenic plants or plants obtained by customary breedingmethods.

The rates of application of active compound are from 0.001 to 3.0,preferably 0.01 to 1.0, kg/ha of active substance (a.s.), depending onthe control target, the season, the target plants and the growth stage.To treat the seed, the compounds of formula I are generally employed inamounts of from 0.001 to 10 kg per 100 kg of seed.

It may also be advantageous to use the compounds of formula I incombination with safeners. Safeners are chemical compounds which preventor reduce damage to useful plants without substantially affecting theherbicidal action of the compounds of formula I on unwanted plants. Theycan be used both before sowing (for example in the treatment of seed, oron cuttings or seedlings) and before or after the emergence of theuseful plant. The safeners and the compounds of formula I can be usedsimultaneously or in succession.

Suitable safeners are, for example, (quinolin-8-oxy)acetic acids,1-phenyl-5-haloalkyl-1H-1,2,4-triazole-3-carboxylic acids,1-phenyl-4,5-dihydro-5-alkyl-1H-pyrazole-3,5-dicarboxylic acids,4,5-dihydro-5,5-diaryl-3-isoxazolecarboxylic acids, dichloroacetamides,alpha-oximinophenylacetonitriles, acetophenone oximes,4,6-dihalo-2-phenylpyrimidines,N-[[4-(aminocarbonyl)phenyl]sulfonyl]-2-benzamides, 1,8-naphthalicanhydride, 2-halo-4-(haloalkyl)-5-thiazolecarboxylic acids,phosphorothiolates and O-phenyl N-alkylcarbamates and theiragriculturally useful salts and, provided that they have an acidfunction, their agriculturally useful derivatives, such as amides,esters and thioesters.

To broaden the activity spectrum and to obtain synergistic effects, thecompounds of the formula I can be mixed and jointly applied withnumerous representatives of other herbicidal or growth-regulating groupsof active compounds or with safeners. Suitable mixing partners are, forexample, 1,2,4-thiadiazoles, 1,3,4-thiadiazoles, amides, aminophosphoricacid and its derivatives, aminotriazoles, anilides,aryloxy/heteroaryloxyalkanoic acids and their derivatives, benzoic acidand its derivatives, benzothiadiazinones,2-(hetaroyl/aroyl)-1,3-cyclohexanediones, heteroaryl aryl ketones,benzylisoxazolidinones, meta-CF₃-phenyl derivatives, carbamates,quinoline carboxylic acid and its derivatives, chloroacetanilides,cyclohexenone oxime ether derivates, diazines, dichloropropionic acidand its derivatives, dihydrobenzofurans, dihydrofu-ran-3-ones,dinitroanilines, dinitrophenols, diphenyl ethers, dipyridyls,halocarboxylic acids and their derivatives, ureas, 3-phenyluracils,imidazoles, imidazolinones, N-phenyl-3,4,5,6-tetrahydrophthalimides,oxadiazoles, oxiranes, phenols, aryloxy- andheteroaryloxyphenoxypro-pionic esters, phenylacetic acid and itsderivatives, 2-phenylpropionic acid and its derivatives, pyrazoles,phenylpyrazoles, pyridazines, pyridinecarboxylic acid and itsderivatives, pyrimidyl ethers, sulfonamides, sulfonylureas, triazines,triazinones, triazolinones, triazolecarboxamides, uracils and alsophenylpyrazolines and isoxazolines and their derivatives.

Moreover, it may be useful to apply the compounds of formula I alone orin combination with other herbicides or else also mixed with furthercrop protection agents, jointly, for example with compositions forcontrolling pests or phytopathogenic fungi or bacteria. Also of interestis the miscibility with mineral salt solutions which are employed foralleviating nutritional and trace element deficiencies. Other additivessuch as nonphytotoxic oils and oil concentrates may also be added.

Examples of herbicides which can be used in combination with theCompounds of formula I according to the present invention are:

b1) from the group of the lipid biosynthesis inhibitors:

alloxydim, alloxydim-sodium, butroxydim, clethodim, clodinafop,clodinafop-propargyl, cycloxydim, cyhalofop, cyhalofop-butyl, diclofop,diclofop-methyl, fenoxaprop, fenoxaprop-ethyl, fenoxaprop-P,fenoxaprop-P-ethyl, fluazifop, fluazifop-butyl, fluazifop-P,fluazifop-P-butyl, haloxyfop, haloxyfop-methyl, haloxyfop-P,haloxyfop-P-methyl, metamifop, pinoxaden, profoxydim, propaquizafop,quizalofop, quizalofop-ethyl, quizalofop-tefuryl, quizalofop-P,quizalofop-P-ethyl, quizalofop-P-tefuryl, sethoxydim, tepraloxydim,tralkoxydim, benfuresate, butylate, cycloate, dalapon, dimepiperate,EPTC, esprocarb, ethofumesate, flupropanate, molinate, orbencarb,pebulate, prosulfocarb, TCA, thiobencarb, tiocarbazil, triallate andvernolate;

b2) from the group of the ALS inhibitors:

amidosulfuron, azimsulfuron, bensulfuron, bensulfuron-methyl,bispyribac, bispyribac-sodium, chlorimuron, chlorimuron-ethyl,chlorsulfuron, cinosulfuron, cloransulam, cloransulam-methyl,cyclosulfamuron, diclosulam, ethametsulfuron, ethametsulfuron-methyl,ethoxysulfuron, flazasulfuron, florasulam, flucarbazone,flucarbazone-sodium, flucetosulfuron, flumetsulam, flupyrsulfuron,flupyrsulfuron-methyl-sodium, foramsulfuron, halosulfuron,halosulfuron-methyl, imazamethabenz, imazamethabenz-methyl, imazamox,imazapic, imazapyr, imazaquin, imazethapyr, imazosulfuron, iodosulfuron,iodosulfuron-methyl-sodium, mesosulfuron, metosulam, metsulfuron,metsulfuron-methyl, nicosulfuron, orthosulfamuron, oxasulfuron,penoxsulam, primisulfuron, primisulfuron-methyl, propoxycarbazone,propoxycarbazone-sodium, prosulfuron, pyrazosulfuron,pyrazosulfuron-ethyl, pyribenzoxim, pyrimisulfan, pyriftalid,pyriminobac, pyriminobac-methyl, pyrithiobac, pyrithiobac-sodium,pyroxsulam, rimsulfuron, sulfometuron, sulfometuron-methyl,sulfosulfuron, thiencarbazone, thiencarbazone-methyl, thifensulfuron,thifensulfuron-methyl, triasulfuron, tribenuron, tribenuron-methyl,trifloxysulfuron, triflusulfuron, triflusulfuron-methyl andtritosulfuron;

b3) from the group of the photosynthesis inhibitors:

ametryn, amicarbazone, atrazine, bentazone, bentazone-sodium, bromacil,bromofenoxim, bromoxynil and its salts and esters, chlorobromuron,chloridazone, chlorotoluron, chloroxuron, cyanazine, desmedipham,desmetryn, dimefuron, dimethametryn, diquat, diquat-dibromide, diuron,fluometuron, hexazinone, ioxynil and its salts and esters, isoproturon,isouron, karbutilate, lenacil, linuron, metamitron, methabenzthiazuron,metobenzuron, metoxuron, metribuzin, monolinuron, neburon, paraquat,paraquat-dichloride, paraquat-dimetilsulfate, pentanochlor,phenmedipham, phenmedipham-ethyl, prometon, prometryn, propanil,propazine, pyridafol, pyridate, siduron, simazine, simetryn,tebuthiuron, terbacil, terbumeton, terbuthylazine, terbutryn,thidiazuron and trietazine;

b4) from the group of the protoporphyrinogen-IX oxidase inhibitors:

acifluorfen, acifluorfen-sodium, azafenidin, bencarbazone,benzfendizone, bifenox, butafenacil, carfentrazone, carfentrazone-ethyl,chlomethoxyfen, cinidon-ethyl, fluazolate, flufenpyr, flufenpyr-ethyl,flumiclorac, flumiclorac-pentyl, flumioxazin, fluoroglycofen,fluoroglycofen-ethyl, fluthiacet, fluthiacet-methyl, fomesafen,halosafen, lactofen, oxadiargyl, oxadiazon, oxyfluorfen, pentoxazone,profluazol, pyraclonil, pyraflufen, pyraflufen-ethyl, saflufenacil,sulfentrazone, thidiazimin,2-chloro-5-[3,6-dihydro-3-methyl-2,6-dioxo-4-(trifluoromethyl)-1(2H)-pyrimidinyl]-4-fluoro-N-[(isopropyl)methylsulfamoyl]benzamide(H-1; CAS 372137-35-4), ethyl[3-[2-chloro-4-fluoro-5-(1-methyl-6-trifluoromethyl-2,4-dioxo-1,2,3,4-tetrahydropyrimidin-3-yl)phenoxy]-2-pyridyloxy]acetate(H-2; CAS 353292-31-6),N-ethyl-3-(2,6-dichloro-4-trifluoromethylphenoxy)-5-methyl-1H-pyrazole-1-carboxamide(H-3; CAS 452098-92-9),N-tetrahydrofurfuryl-3-(2,6-dichloro-4-trifluoromethylphenoxy)-5-methyl-1H-pyrazole-1-carboxamide(H-4; CAS 915396-43-9),N-ethyl-3-(2-chloro-6-fluoro-4-trifluoromethylphenoxy)-5-methyl-1H-pyrazole-1-carboxamide(H-5; CAS 452099-05-7),N-tetrahydrofurfuryl-3-(2-chloro-6-fluoro-4-trifluoromethylphenoxy)-5-methyl-1H-pyrazole-1-carboxamide(H-6; CAS 45100-03-7),3-[7-fluoro-3-oxo-4-(prop-2-ynyl)-3,4-dihydro-2H-benzo[1,4]oxazin-6-yl]-1,5-dimethyl-6-thioxo-[1,3,5]triazinan-2,4-dione,1,5-dimethyl-6-thioxo-3-(2,2,7-trifluoro-3-oxo-4-(prop-2-ynyl)-3,4-dihydro-2H-benzo[b][1,4]oxazin-6-yl)-1,3,5-triazinane-2,4-dione,2-(2,2,7-Trifluoro-3-oxo-4-prop-2-ynyl-3,4-dihydro-2H-benzo[1,4]oxazin-6-yl)-4,5,6,7-tetrahydro-isoindole-1,3-dioneand1-Methyl-6-trifluoromethyl-3-(2,2,7-trifluoro-3-oxo-4-prop-2-ynyl-3,4-dihydro-2H-benzo[1,4]oxazin-6-yl)-1H-pyrimidine-2,4-dione;

b5) from the group of the bleacher herbicides:

aclonifen, amitrol, beflubutamid, benzobicyclon, benzofenap, clomazone,diflufenican, fluridone, flurochloridone, flurtamone, isoxaflutole,mesotrione, norflurazon, picolinafen, pyrasulfutole, pyrazolynate,pyrazoxyfen, sulcotrione, tefuryltrione, tembotrione, topramezone,4-hydroxy-3-[[2-[(2-methoxyethoxy)methyl]-6-(trifluoromethyl)-3-pyridyl]carbonyl]bicyclo[3.2.1]oct-3-en-2-one(H-7; CAS 352010-68-5) and4-(3-trifluoromethylphenoxy)-2-(4-trifluoromethylphenyl)pyrimidine (H-8;CAS 180608-33-7);

b6) from the group of the EPSP synthase inhibitors:

glyphosate, glyphosate-isopropylammonium and glyphosate-trimesium(sulfosate);

b7) from the group of the glutamine synthase inhibitors:

bilanaphos (bialaphos), bilanaphos-sodium, glufosinate andglufosinate-ammonium;

b8) from the group of the DHP synthase inhibitors:

asulam;

b9) from the group of the mitose inhibitors:

amiprophos, amiprophos-methyl, benfluralin, butamiphos, butralin,carbetamide, chlorpropham, chlorthal, chlorthal-dimethyl, dinitramine,dithiopyr, ethalfluralin, fluchloralin, oryzalin, pendimethalin,prodiamine, propham, propyzamide, tebutam, thiazopyr and trifluralin;

b10) from the group of the VLCFA inhibitors:

acetochlor, alachlor, anilofos, butachlor, cafenstrole, dimethachlor,dimethanamid, dimethenamid-P, diphenamid, fentrazamide, flufenacet,mefenacet, metazachlor, metolachlor, metolachlor-S, naproanilide,napropamide, pethoxamid, piperophos, pretilachlor, propachlor,propisochlor, pyroxasulfone (KIH-485) and thenylchlor;

Compounds of the Formula 2:

in which the variables have the following meanings:Y is phenyl or 5- or 6-membered heteroaryl as defined at the outset,which radicals may be substituted by one to three groups R^(aa); R^(A),R^(B), R^(C), R^(D) are H, halogen or C₁-C₄-alkyl; A is O or NH; q is 0or 1.

Compounds of the formula 2 have in particular the following meanings:

-   -   Y is

where # denotes the bond to the skeleton of the molecule; and R^(A),R^(B), R^(C), R^(D) are H, Cl, F or CH₃; R^(E) is halogen, C₁-C₄-alkylor C₁-C₄-haloalkyl; R^(F) is C₁-C₄-alkyl; R^(G) is halogen, C₁-C₄-alkoxyor C₁-C₄-haloalkoxy; R^(H) is H, halogen, C₁-C₄-alkyl, C₁-C₄-haloalkylor C₁-C₄-haloalkoxy; r is 0, 1, 2 or 3; A is oxygen; q is 0 or 1.

Preferred compounds of the formula 2 have the following meanings:

R^(A) is H; R^(B), R^(C) are F; R²⁴ is H or F; A is oxygen; q is 0 or 1.

Particularly preferred compounds of the formula 2 are:

3-[5-(2,2-difluoroethoxy)-1-methyl-3-trifluoromethyl-1H-pyrazol-4-ylmethane-sulfonyl]-4-fluoro-5,5-dimethyl-4,5-dihydroisoxazole(2-1);3-{[5-(2,2-difluoroethoxy)-1-methyl-3-trifluoromethyl-1H-pyrazol-4-yl]fluoromethanesulfonyl}-5,5-dimethyl-4,5-dihydroisoxazole(2-2);4-(4-fluoro-5,5-dimethyl-4,5-dihydroisoxazole-3-sulfonylmethyl)-2-methyl-5-trifluoromethyl-2H-[1,2,3]triazole(2-3);4-[(5,5-dimethyl-4,5-dihydroisoxazole-3-sulfonyl)fluoromethyl]-2-methyl-5-trifluoromethyl-2H-[1,2,3]triazole(2-4);4-(5,5-dimethyl-4,5-dihydroisoxazole-3-sulfonylmethyl)-2-methyl-5-trifluoromethyl-2H-[1,2,3]triazole(2-5);3-{[5-(2,2-difluoroethoxy)-1-methyl-3-trifluoromethyl-1H-pyrazol-4-yl]difluoromethanesulfonyl}-5,5-dimethyl-4,5-dihydroisoxazole(2-6);4-[(5,5-dimethyl-4,5-dihydroisoxazole-3-sulfonyl)difluoromethyl]-2-methyl-5-trifluoromethyl-2H-[1,2,3]triazole(2-7);3-{[5-(2,2-difluoroethoxy)-1-methyl-3-trifluoromethyl-1H-pyrazol-4-yl]difluoromethanesulfonyl}-4-fluoro-5,5-dimethyl-4,5-dihydroisoxazole(2-8);4-[difluoro-(4-fluoro-5,5-dimethyl-4,5-dihydroisoxazole-3-sulfonyl)methyl]-2-methyl-5-trifluoromethyl-2H-[1,2,3]triazole(2-9);

b11) from the group of the cellulose biosynthesis inhibitors:

chlorthiamid, dichlobenil, flupoxam and isoxaben;

b12) from the group of the decoupler herbicides:

dinoseb, dinoterb and DNOC and its salts;

b13) from the group of the auxin herbicides:

2,4-D and its salts and esters, 2,4-DB and its salts and esters,aminopyralid and its salts such asaminopyralid-tris(2-hydroxypropyl)ammonium and its esters, benazolin,benazolin-ethyl, chloramben and its salts and esters, clomeprop,clopyralid and its salts and esters, dicamba and its salts and esters,dichlorprop and its salts and esters, dichlorprop-P and its salts andesters, fluroxypyr, fluroxypyr-butometyl, fluroxypyr-meptyl, MCPA andits salts and esters, MCPA-thioethyl, MCPB and its salts and esters,mecoprop and its salts and esters, mecoprop-P and its salts and esters,picloram and its salts and esters, quinclorac, quinmerac, TBA (2,3,6)and its salts and esters, triclopyr and its salts and esters, and5,6-dichloro-2-cyclopropyl-4-pyrimidinecarboxylic acid (H-9; CAS858956-08-8) and its salts and esters;

b14) from the group of the auxin transport inhibitors: diflufenzopyr,diflufenzopyr-sodium, naptalam and naptalam-sodium;

b15) from the group of the other herbicides: bromobutide, chlorflurenol,chlorflurenol-methyl, cinmethylin, cumyluron, dalapon, dazomet,difenzoquat, difenzoquat-metilsulfate, dimethipin, DSMA, dymron,endothal and its salts, etobenzanid, flamprop, flamprop-isopropyl,flamprop-methyl, flamprop-M-isopropyl, flamprop-M-methyl, flurenol,flurenol-butyl, flurprimidol, fosamine, fosamine-ammonium, indanofan,maleic hydrazide, mefluidide, metam, methyl azide, methyl bromide,methyl-dymron, methyl iodide, MSMA, oleic acid, oxaziclomefone,pelargonic acid, pyributicarb, quinoclamine, triaziflam, tridiphane and6-chloro-3-(2-cyclopropyl-6-methylphenoxy)-4-pyridazinol (H-10; CAS499223-49-3) and its salts and esters.

Examples of preferred safeners C are benoxacor, cloquintocet,cyometrinil, cyprosulfamide, dichlormid, dicyclonone, dietholate,fenchlorazole, fenclorim, flurazole, fluxofenim, furi-lazole,isoxadifen, mefenpyr, mephenate, naphthalic anhydride, oxabetrinil,4-(dichloroacetyl)-1-oxa-4-azaspiro[4.5]decane (H-11; MON4660, CAS71526-07-3) and 2,2,5-trimethyl-3-(dichloroacetyl)-1,3-oxazolidine(H-12; R-29148, CAS 52836-31-4).

The active compounds of groups b1) to b15) and the safeners C are knownherbicides and safeners, see, for example, The Compendium of PesticideCommon Names (http://www.alanwood.net/pesticides/); B. Hock, C. Fedtke,R. R. Schmidt, Herbizide [Herbicides], Georg Thieme Verlag, Stuttgart,1995. Further herbicidally active compounds are known from WO 96/26202,WO 97/41116, WO 97/41117, WO 97/41118, WO 01/83459 and WO 2008/074991and from W. Kramer et al. (ed.) “Modern Crop Protection Compounds”, Vol.1, Wiley VCH, 2007 and the literature quoted therein.

The invention also relates to compositions in the form of a cropprotection composition formulated as a 1-component compositioncomprising an active compound combination comprising at least onecompound of the formula I and at least one further active compound,preferably selected from the active compounds of groups b1 to b15, andat least one solid or liquid carrier and/or one or more surfactants and,if desired, one or more further auxiliaries customary for cropprotection compositions.

The invention also relates to compositions in the form of a cropprotection composition formulated as a 2-component compositioncomprising a first component comprising at least one compound of theformula I, a solid or liquid carrier and/or one or more surfactants anda second component comprising at least one further active compoundselected from the active compounds of groups b1 to b15, a solid orliquid carrier and/or one or more surfactants, where additionally bothcomponents may also comprise further auxiliaries customary for cropprotection compositions.

In binary compositions comprising at least one compound of the formula Ias component A and at least one herbicide B, the weight ratio of theactive compounds A:B is generally in the range of from 1:1000 to 1000:1,preferably in the range of from 1:500 to 500:1, in particular in therange of from 1:250 to 250:1 and particularly preferably in the range offrom 1:75 to 75:1.

In binary compositions comprising at least one compound of the formula Ias component A and at least one safener C, the weight ratio of theactive compounds A:C is generally in the range of from 1:1000 to 1000:1,preferably in the range of from 1:500 to 500:1, in particular in therange of from 1:250 to 250:1 and particularly preferably in the range offrom 1:75 to 75:1.

In ternary compositions comprising both at least one compound of theformula I as component A, at least one herbicide B and at least onesafener C, the relative parts by weight of the components A:B aregenerally in the range of from 1:1000 to 1000:1, preferably in the rangeof from 1:500 to 500:1, in particular in the range of from 1:250 to250:1 and particularly preferably in the range of from 1:75 to 75:1; theweight ratio of the components A:C is generally in the range of from1:1000 to 1000:1, preferably in the range of from 1:500 to 500:1, inparticular in the range of from 1:250 to 250:1 and particularlypreferably in the range of from 1:75 to 75:1; and the weight ratio ofthe components B:C is generally in the range of from 1:1000 to 1000:1,preferably in the range of from 1:500 to 500:1, in particular in therange of from 1:250 to 250:1 and particularly preferably in the range offrom 1:75 to 75:1. Preferably, the weight ratio of the components A+B tothe component C is in the range of from 1:500 to 500:1, in particular inthe range of from 1:250 to 250:1 and particularly preferably in therange of from 1:75 to 75:1.

Examples of particularly preferred compositions according to theinvention comprising in each case one individualized compound of theformula I and one mixing partner or a mixing partner combination aregiven in Table B below.

A further aspect of the invention relates to the compositions B-1 toB-1236 listed in Table B below, where in each case one row of Table Bcorresponds to a herbicidal composition comprising one of the compoundsof formula I individualized in the above description (component 1) andthe further active compound from groups b1) to b15) and/or safener Cstated in each case in the row in question (component 2). The activecompounds in the compositions described are in each case preferablypresent in synergistically effective amounts.

TABLE B Herbicide(s) B Safener C B-1 clodinafop-propargyl — B-2cycloxydim — B-3 cyhalofop-butyl — B-4 fenoxaprop-P-ethyl — B-5pinoxaden — B-6 profoxydim — B-7 tepraloxydim — B-8 tralkoxydim — B-9esprocarb — B-10 prosulfocarb — B-11 thiobencarb — B-12 triallate — B-13bensulfuron-methyl — B-14 bispyribac-sodium — B-15 cyclosulfamuron —B-16 flumetsulam — B-17 flupyrsulfuron-methyl-sodium — B-18foramsulfuron — B-19 imazamox — B-20 imazapic — B-21 imazapyr — B-22imazaquin — B-23 imazethapyr — B-24 imazosulfuron — B-25iodosulfuron-methyl-sodium — B-26 mesosulfuron — B-27 nicosulfuron —B-28 penoxsulam — B-29 propoxycarbazone-sodium — B-30pyrazosulfuron-ethyl — B-31 pyroxsulam — B-32 rimsulfuron — B-33sulfosulfuron — B-34 thiencarbazone-methyl — B-35 tritosulfuron — B-362,4-D and its salts and esters — B-37 aminopyralid and its salts andesters — B-38 clopyralid and its salts and esters — B-39 dicamba and itssalts and esters — B-40 fluroxypyr-meptyl — B-41 quinclorac — B-42quinmerac — B-43 H-9 — B-44 diflufenzopyr — B-45 diflufenzopyr-sodium —B-46 clomazone — B-47 diflufenican — B-48 fluorochloridone — B-49isoxaflutol — B-50 mesotrione — B-51 picolinafen — B-52 sulcotrione —B-53 tefuryltrione — B-54 tembotrione — B-55 topramezone — B-56 H-7 —B-57 atrazine — B-58 diuron — B-59 fluometuron — B-60 hexazinone — B-61isoproturon — B-62 metribuzin — B-63 propanil — B-64 terbuthylazine —B-65 paraquat dichloride — B-66 flumioxazin — B-67 oxyfluorfen — B-68saflufenacil — B-69 sulfentrazone — B-70 H-1 — B-71 H-2 — B-72glyphosate — B-73 glyphosate-isopropylammonium — B-74glyphosate-trimesium (sulfosate) — B-75 glufosinate — B-76glufosinate-ammonium — B-77 pendimethalin — B-78 trifluralin — B-79acetochlor — B-80 cafenstrole — B-81 dimethenamid-P — B-82 fentrazamide— B-83 flufenacet — B-84 mefenacet — B-85 metazachlor — B-86metolachlor-S — B-87 pyroxasulfone — B-88 isoxaben — B-89 dymron — B-90indanofan — B-91 oxaziclomefone — B-92 triaziflam — B-93 chlorotoluron —B-94 atrazine + H-1 — B-95 atrazine + glyphosate — B-96 atrazine +mesotrione — B-97 atrazine + nicosulfuron — B-98 atrazine + tembotrione— B-99 atrazine + topramezone — B-100 clomazone + glyphosate — B-101diflufenican + clodinafop-propargyl — B-102 diflufenican +fenoxaprop-P-ethyl — B-103 diflufenican + flupyrsulfuron-methyl-sodium —B-104 diflufenican + glyphosate — B-105 diflufenican +mesosulfuron-methyl — B-106 diflufenican + pinoxaden — B-107diflufenican + pyroxsulam — B-108 flumetsulam + glyphosate — B-109flumioxazin + glyphosate — B-110 imazapic + glyphosate — B-111imazethapyr + glyphosate — B-112 isoxaflutol + H-1 — B-113 isoxaflutol +glyphosate — B-114 metazachlor + H-1 — B-115 metazachlor + glyphosate —B-116 metazachlor + mesotrione — B-117 metazachlor + nicosulfuron —B-118 metazachlor + terbuthylazine — B-119 metazachlor + topramezone —B-120 metribuzin + glyphosate — B-121 pendimethalin + H-1 — B-122pendimethalin + clodinafop-propargyl — B-123 pendimethalin +fenoxaprop-P-ethyl — B-124 pendimethalin + flupyrsulfuron-methyl-sodium— B-125 pendimethalin + glyphosate — B-126 pendimethalin +mesosulfuron-methyl — B-127 pendimethalin + mesotrione — B-128pendimethalin + nicosulfuron — B-129 pendimethalin + pinoxaden — B-130pendimethalin + pyroxsulam — B-131 pendimethalin + tembotrione — B-132pendimethalin + topramezone — B-133 pyroxasulfone + tembotrione — B-134pyroxasulfone + topramezone — B-135 sulfentrazone + glyphosate — B-136terbuthylazine + H-1 — B-137 terbuthylazine + foramsulfuron — B-138terbuthylazine + glyphosate — B-139 terbuthylazine + mesotrione — B-140terbuthylazine + nicosulfuron — B-141 terbuthylazine + tembotrione —B-142 terbuthylazine + topramezone — B-143 trifluralin + glyphosate —B-144 — benoxacor B-145 — cloquintocet B-146 — cyprosulfamide B-147 —dichlormid B-148 — fenchlorazole B-149 — isoxadifen B-150 — mefenpyrB-151 — H-11 B-152 — H-12 B-153 clodinafop-propargyl benoxacor B-154cycloxydim benoxacor B-155 cyhalofop-butyl benoxacor B-156fenoxaprop-P-ethyl benoxacor B-157 pinoxaden benoxacor B-158 profoxydimbenoxacor B-159 tepraloxydim benoxacor B-160 tralkoxydim benoxacor B-161esprocarb benoxacor B-162 prosulfocarb benoxacor B-163 thiobencarbbenoxacor B-164 triallate benoxacor B-165 bensulfuron-methyl benoxacorB-166 bispyribac-sodium benoxacor B-167 cyclosulfamuron benoxacor B-168flumetsulam benoxacor B-169 flupyrsulfuron-methyl-sodium benoxacor B-170foramsulfuron benoxacor B-171 imazamox benoxacor B-172 imazapicbenoxacor B-173 imazapyr benoxacor B-174 imazaquin benoxacor B-175imazethapyr benoxacor B-176 imazosulfuron benoxacor B-177iodosulfuron-methyl-sodium benoxacor B-178 mesosulfuron benoxacor B-179nicosulfuron benoxacor B-180 penoxsulam benoxacor B-181propoxycarbazone-sodium benoxacor B-182 pyrazosulfuron-ethyl benoxacorB-183 pyroxsulam benoxacor B-184 rimsulfuron benoxacor B-185sulfosulfuron benoxacor B-186 thiencarbazone-methyl benoxacor B-187tritosulfuron benoxacor B-188 2,4-D and its salts and esters benoxacorB-189 aminopyralid and its salts and esters benoxacor B-190 clopyralidand its salts and esters benoxacor B-191 dicamba and its salts andesters benoxacor B-192 fluroxypyr-meptyl benoxacor B-193 quincloracbenoxacor B-194 quinmerac benoxacor B-195 H-9 benoxacor B-196diflufenzopyr benoxacor B-197 diflufenzopyr-sodium benoxacor B-198clomazone benoxacor B-199 diflufenican benoxacor B-200 fluorochloridonebenoxacor B-201 isoxaflutol benoxacor B-202 mesotrione benoxacor B-203picolinafen benoxacor B-204 sulcotrione benoxacor B-205 tefuryltrionebenoxacor B-206 tembotrione benoxacor B-207 topramezone benoxacor B-208H-7 benoxacor B-209 atrazine benoxacor B-210 diuron benoxacor B-211fluometuron benoxacor B-212 hexazinone benoxacor B-213 isoproturonbenoxacor B-214 metribuzin benoxacor B-215 propanil benoxacor B-216terbuthylazine benoxacor B-217 paraquat dichloride benoxacor B-218flumioxazin benoxacor B-219 oxyfluorfen benoxacor B-220 saflufenacilbenoxacor B-221 sulfentrazone benoxacor B-222 H-1 benoxacor B-223 H-2benoxacor B-224 glyphosate benoxacor B-225 glyphosate-isopropylammoniumbenoxacor B-226 glyphosate-trimesium (sulfosate) benoxacor B-227glufosinate benoxacor B-228 glufosinate-ammonium benoxacor B-229pendimethalin benoxacor B-230 trifluralin benoxacor B-231 acetochlorbenoxacor B-232 cafenstrole benoxacor B-233 dimethenamid-P benoxacorB-234 fentrazamide benoxacor B-235 flufenacet benoxacor B-236 mefenacetbenoxacor B-237 metazachlor benoxacor B-238 metolachlor-S benoxacorB-239 pyroxasulfone benoxacor B-240 isoxaben benoxacor B-241 dymronbenoxacor B-242 indanofan benoxacor B-243 oxaziclomefone benoxacor B-244triaziflam benoxacor B-245 atrazine + H-1 benoxacor B-246 atrazine +glyphosate benoxacor B-247 atrazine + mesotrione benoxacor B-248atrazine + nicosulfuron benoxacor B-249 atrazine + tembotrione benoxacorB-250 atrazine + topramezone benoxacor B-251 clomazone + glyphosatebenoxacor B-252 diflufenican + clodinafop-propargyl benoxacor B-253diflufenican + fenoxaprop-P-ethyl benoxacor B-254 diflufenican +flupyrsulfuron-methyl-sodium benoxacor B-255 diflufenican + glyphosatebenoxacor B-256 diflufenican + mesosulfuron-methyl benoxacor B-257diflufenican + pinoxaden benoxacor B-258 diflufenican + pyroxsulambenoxacor B-259 flumetsulam + glyphosate benoxacor B-260 flumioxazin +glyphosate benoxacor B-261 imazapic + glyphosate benoxacor B-262imazethapyr + glyphosate benoxacor B-263 isoxaflutol + H-1 benoxacorB-264 isoxaflutol + glyphosate benoxacor B-265 metazachlor + H-1benoxacor B-266 metazachlor + glyphosate benoxacor B-267 metazachlor +mesotrione benoxacor B-268 metazachlor + nicosulfuron benoxacor B-269metazachlor + terbuthylazine benoxacor B-270 metazachlor + topramezonebenoxacor B-271 metribuzin + glyphosate benoxacor B-272 pendimethalin +H-1 benoxacor B-273 pendimethalin + clodinafop-propargyl benoxacor B-274pendimethalin + fenoxaprop-P-ethyl benoxacor B-275 pendimethalin +flupyrsulfuron-methyl-sodium benoxacor B-276 pendimethalin + glyphosatebenoxacor B-277 pendimethalin + mesosulfuron-methyl benoxacor B-278pendimethalin + mesotrione benoxacor B-279 pendimethalin + nicosulfuronbenoxacor B-280 pendimethalin + pinoxaden benoxacor B-281pendimethalin + pyroxsulam benoxacor B-282 pendimethalin + tembotrionebenoxacor B-283 pendimethalin + topramezone benoxacor B-284pyroxasulfone + tembotrione benoxacor B-285 pyroxasulfone + topramezonebenoxacor B-286 sulfentrazone + glyphosate benoxacor B-287terbuthylazine + H-1 benoxacor B-288 terbuthylazine + foramsulfuronbenoxacor B-289 terbuthylazine + glyphosate benoxacor B-290terbuthylazine + mesotrione benoxacor B-291 terbuthylazine +nicosulfuron benoxacor B-292 terbuthylazine + tembotrione benoxacorB-293 terbuthylazine + topramezone benoxacor B-294 trifluralin +glyphosate benoxacor B-295 clodinafop-propargyl cloquintocet B-296cycloxydim cloquintocet B-297 cyhalofop-butyl cloquintocet B-298fenoxaprop-P-ethyl cloquintocet B-299 pinoxaden cloquintocet B-300profoxydim cloquintocet B-301 tepraloxydim cloquintocet B-302tralkoxydim cloquintocet B-303 esprocarb cloquintocet B-304 prosulfocarbcloquintocet B-305 thiobencarb cloquintocet B-306 triallate cloquintocetB-307 bensulfuron-methyl cloquintocet B-308 bispyribac-sodiumcloquintocet B-309 cyclosulfamuron cloquintocet B-310 flumetsulamcloquintocet B-311 flupyrsulfuron-methyl-sodium cloquintocet B-312foramsulfuron cloquintocet B-313 imazamox cloquintocet B-314 imazapiccloquintocet B-315 imazapyr cloquintocet B-316 imazaquin cloquintocetB-317 imazethapyr cloquintocet B-318 imazosulfuron cloquintocet B-319iodosulfuron-methyl-sodium cloquintocet B-320 mesosulfuron cloquintocetB-321 nicosulfuron cloquintocet B-322 penoxsulam cloquintocet B-323propoxycarbazone-sodium cloquintocet B-324 pyrazosulfuron-ethylcloquintocet B-325 pyroxsulam cloquintocet B-326 rimsulfuroncloquintocet B-327 sulfosulfuron cloquintocet B-328thiencarbazone-methyl cloquintocet B-329 tritosulfuron cloquintocetB-330 2,4-D and its salts and esters cloquintocet B-331 aminopyralid andits salts and esters cloquintocet B-332 clopyralid and its salts andesters cloquintocet B-333 dicamba and its salts and esters cloquintocetB-334 fluroxypyr-meptyl cloquintocet B-335 quinclorac cloquintocet B-336quinmerac cloquintocet B-337 H-9 cloquintocet B-338 diflufenzopyrcloquintocet B-339 diflufenzopyr-sodium cloquintocet B-340 clomazonecloquintocet B-341 diflufenican cloquintocet B-342 fluorochloridonecloquintocet B-343 isoxaflutol cloquintocet B-344 mesotrionecloquintocet B-345 picolinafen cloquintocet B-346 sulcotrionecloquintocet B-347 tefuryltrione cloquintocet B-348 tembotrionecloquintocet B-349 topramezone cloquintocet B-350 H-7 cloquintocet B-351atrazine cloquintocet B-352 diuron cloquintocet B-353 fluometuroncloquintocet B-354 hexazinone cloquintocet B-355 isoproturoncloquintocet B-356 metribuzin cloquintocet B-357 propanil cloquintocetB-358 terbuthylazine cloquintocet B-359 paraquat dichloride cloquintocetB-360 flumioxazin cloquintocet B-361 oxyfluorfen cloquintocet B-362saflufenacil cloquintocet B-363 sulfentrazone cloquintocet B-364 H-1cloquintocet B-365 H-2 cloquintocet B-366 glyphosate cloquintocet B-367glyphosate-isopropylammonium cloquintocet B-368 glyphosate-trimesium(sulfosate) cloquintocet B-369 glufosinate cloquintocet B-370glufosinate-ammonium cloquintocet B-371 pendimethalin cloquintocet B-372trifluralin cloquintocet B-373 acetochlor cloquintocet B-374 cafenstrolecloquintocet B-375 dimethenamid-P cloquintocet B-376 fentrazamidecloquintocet B-377 flufenacet cloquintocet B-378 mefenacet cloquintocetB-379 metazachlor cloquintocet B-380 metolachlor-S cloquintocet B-381pyroxasulfone cloquintocet B-382 isoxaben cloquintocet B-383 dymroncloquintocet B-384 indanofan cloquintocet B-385 oxaziclomefonecloquintocet B-386 triaziflam cloquintocet B-387 atrazine + H-1cloquintocet B-388 atrazine + glyphosate cloquintocet B-389 atrazine +mesotrione cloquintocet B-390 atrazine + nicosulfuron cloquintocet B-391atrazine + tembotrione cloquintocet B-392 atrazine + topramezonecloquintocet B-393 clomazone + glyphosate cloquintocet B-394diflufenican + clodinafop-propargyl cloquintocet B-395 diflufenican +fenoxaprop-p-ethyl cloquintocet B-396 diflufenican +flupyrsulfuron-methyl-sodium cloquintocet B-397 diflufenican +glyphosate cloquintocet B-398 diflufenican + mesosulfuron-methylcloquintocet B-399 diflufenican + pinoxaden cloquintocet B-400diflufenican + pyroxsulam cloquintocet B-401 flumetsulam + glyphosatecloquintocet B-402 flumioxazin + glyphosate cloquintocet B-403imazapic + glyphosate cloquintocet B-404 imazethapyr + glyphosatecloquintocet B-405 isoxaflutol + H-1 cloquintocet B-406 isoxaflutol +glyphosate cloquintocet B-407 metazachlor + H-1 cloquintocet B-408metazachlor + glyphosate cloquintocet B-409 metazachlor + mesotrionecloquintocet B-410 metazachlor + nicosulfuron cloquintocet B-411metazachlor + terbuthylazine cloquintocet B-412 metazachlor +topramezone cloquintocet B-413 metribuzin + glyphosate cloquintocetB-414 pendimethalin + H-1 cloquintocet B-415 pendimethalin +clodinafop-propargyl cloquintocet B-416 pendimethalin +fenoxaprop-P-ethyl cloquintocet B-417 pendimethalin +flupyrsulfuron-methyl-sodium cloquintocet B-418 pendimethalin +glyphosate cloquintocet B-419 pendimethalin + mesosulfuron-methylcloquintocet B-420 pendimethalin + mesotrione cloquintocet B-421pendimethalin + nicosulfuron cloquintocet B-422 pendimethalin +pinoxaden cloquintocet B-423 pendimethalin + pyroxsulam cloquintocetB-424 pendimethalin + tembotrione cloquintocet B-425 pendimethalin +topramezone cloquintocet B-426 pyroxasulfone + tembotrione cloquintocetB-427 pyroxasulfone + topramezone cloquintocet B-428 sulfentrazone +glyphosate cloquintocet B-429 terbuthylazine + H-1 cloquintocet B-430terbuthylazine + foramsulfuron cloquintocet B-431 terbuthylazine +glyphosate cloquintocet B-432 terbuthylazine + mesotrione cloquintocetB-433 terbuthylazine + nicosulfuron cloquintocet B-434 terbuthylazine +tembotrione cloquintocet B-435 terbuthylazine + topramezone cloquintocetB-436 trifluralin + glyphosate cloquintocet B-437 clodinafop-propargyldichlormid B-438 cycloxydim dichlormid B-439 cyhalofop-butyl dichlormidB-440 fenoxaprop-P-ethyl dichlormid B-441 pinoxaden dichlormid B-442profoxydim dichlormid B-443 tepraloxydim dichlormid B-444 tralkoxydimdichlormid B-445 esprocarb dichlormid B-446 prosulfocarb dichlormidB-447 thiobencarb dichlormid B-448 triallate dichlormid B-449bensulfuron-methyl dichlormid B-450 bispyribac-sodium dichlormid B-451cyclosulfamuron dichlormid B-452 flumetsulam dichlormid B-453flupyrsulfuron-methyl-sodium dichlormid B-454 foramsulfuron dichlormidB-455 imazamox dichlormid B-456 imazapic dichlormid B-457 imazapyrdichlormid B-458 imazaquin dichlormid B-459 imazethapyr dichlormid B-460imazosulfuron dichlormid B-461 iodosulfuron-methyl-sodium dichlormidB-462 mesosulfuron dichlormid B-463 nicosulfuron dichlormid B-464penoxsulam dichlormid B-465 propoxycarbazone-sodium dichlormid B-466pyrazosulfuron-ethyl dichlormid B-467 pyroxsulam dichlormid B-468rimsulfuron dichlormid B-469 sulfosulfuron dichlormid B-470thiencarbazone-methyl dichlormid B-471 tritosulfuron dichlormid B-4722,4-D and its salts and esters dichlormid B-473 aminopyralid and itssalts and esters dichlormid B-474 clopyralid and its salts and estersdichlormid B-475 dicamba and its salts and esters dichlormid B-476fluroxypyr-meptyl dichlormid B-477 quinclorac dichlormid B-478 quinmeracdichlormid B-479 H-9 dichlormid B-480 diflufenzopyr dichlormid B-481diflufenzopyr-sodium dichlormid B-482 clomazone dichlormid B-483diflufenican dichlormid B-484 fluorochloridone dichlormid B-485isoxaflutol dichlormid B-486 mesotrione dichlormid B-487 picolinafendichlormid B-488 sulcotrione dichlormid B-489 tefuryltrione dichlormidB-490 tembotrione dichlormid B-491 topramezone dichlormid B-492 H-7dichlormid B-493 atrazine dichlormid B-494 diuron dichlormid B-495fluometuron dichlormid B-496 hexazinone dichlormid B-497 isoproturondichlormid B-498 metribuzin dichlormid B-499 propanil dichlormid B-500terbuthylazine dichlormid B-501 paraquat dichloride dichlormid B-502flumioxazin dichlormid B-503 oxyfluorfen dichlormid B-504 saflufenacildichlormid B-505 sulfentrazone dichlormid B-506 H-1 dichlormid B-507 H-2dichlormid B-508 glyphosate dichlormid B-509glyphosate-isopropylammonium dichlormid B-510 glyphosate-trimesium(sulfosate) dichlormid B-511 glufosinate dichlormid B-512glufosinate-ammonium dichlormid B-513 pendimethalin dichlormid B-514trifluralin dichlormid B-515 acetochlor dichlormid B-516 cafenstroledichlormid B-517 dimethenamid-P dichlormid B-518 fentrazamide dichlormidB-519 flufenacet dichlormid B-520 mefenacet dichlormid B-521 metazachlordichlormid B-522 metolachlor-S dichlormid B-523 pyroxasulfone dichlormidB-524 isoxaben dichlormid B-525 dymron dichlormid B-526 indanofandichlormid B-527 oxaziclomefone dichlormid B-528 triaziflam dichlormidB-529 atrazine + H-1 dichlormid B-530 atrazine + glyphosate dichlormidB-531 atrazine + mesotrione dichlormid B-532 atrazine + nicosulfurondichlormid B-533 atrazine + tembotrione dichlormid B-534 atrazine +topramezone dichlormid B-535 clomazone + glyphosate dichlormid B-536diflufenican + clodinafop-propargyl dichlormid B-537 diflufenican +fenoxaprop-p-ethyl dichlormid B-538 diflufenican +flupyrsulfuron-methyl-sodium dichlormid B-539 diflufenican + glyphosatedichlormid B-540 diflufenican + mesosulfuron-methyl dichlormid B-541diflufenican + pinoxaden dichlormid B-542 diflufenican + pyroxsulamdichlormid B-543 flumetsulam + glyphosate dichlormid B-544 flumioxazin +glyphosate dichlormid B-545 imazapic + glyphosate dichlormid B-546imazethapyr + glyphosate dichlormid B-547 isoxaflutol + H-1 dichlormidB-548 isoxaflutol + glyphosate dichlormid B-549 metazachlor + H-1dichlormid B-550 metazachlor + glyphosate dichlormid B-551 metazachlor +mesotrione dichlormid B-552 metazachlor + nicosulfuron dichlormid B-553metazachlor + terbuthylazine dichlormid B-554 metazachlor + topramezonedichlormid B-555 metribuzin + glyphosate dichlormid B-556pendimethalin + H-1 dichlormid B-557 pendimethalin +clodinafop-propargyl dichlormid B-558 pendimethalin + fenoxaprop-P-ethyldichlormid B-559 pendimethalin + flupyrsulfuron-methyl-sodium dichlormidB-560 pendimethalin + glyphosate dichlormid B-561 pendimethalin +mesosulfuron-methyl dichlormid B-562 pendimethalin + mesotrionedichlormid B-563 pendimethalin + nicosulfuron dichlormid B-564pendimethalin + pinoxaden dichlormid B-565 pendimethalin + pyroxsulamdichlormid B-566 pendimethalin + tembotrione dichlormid B-567pendimethalin + topramezone dichlormid B-568 pyroxasulfone + tembotrionedichlormid B-569 pyroxasulfone + topramezone dichlormid B-570sulfentrazone + glyphosate dichlormid B-571 terbuthylazine + H-1dichlormid B-572 terbuthylazine + foramsulfuron dichlormid B-573terbuthylazine + glyphosate dichlormid B-574 terbuthylazine + mesotrionedichlormid B-575 terbuthylazine + nicosulfuron dichlormid B-576terbuthylazine + tembotrione dichlormid B-577 terbuthylazine +topramezone dichlormid B-578 trifluralin + glyphosate dichlormid B-579clodinafop-propargyl fenchlorazole B-580 cycloxydim fenchlorazole B-581cyhalofop-butyl fenchlorazole B-582 fenoxaprop-P-ethyl fenchlorazoleB-583 pinoxaden fenchlorazole B-584 profoxydim fenchlorazole B-585tepraloxydim fenchlorazole B-586 tralkoxydim fenchlorazole B-587esprocarb fenchlorazole B-588 prosulfocarb fenchlorazole B-589thiobencarb fenchlorazole B-590 triallate fenchlorazole B-591bensulfuron-methyl fenchlorazole B-592 bispyribac-sodium fenchlorazoleB-593 cyclosulfamuron fenchlorazole B-594 flumetsulam fenchlorazoleB-595 flupyrsulfuron-methyl-sodium fenchlorazole B-596 foramsulfuronfenchlorazole B-597 imazamox fenchlorazole B-598 imazapic fenchlorazoleB-599 imazapyr fenchlorazole B-600 imazaquin fenchlorazole B-601imazethapyr fenchlorazole B-602 imazosulfuron fenchlorazole B-603iodosulfuron-methyl-sodium fenchlorazole B-604 mesosulfuronfenchlorazole B-605 nicosulfuron fenchlorazole B-606 penoxsulamfenchlorazole B-607 propoxycarbazone-sodium fenchlorazole B-608pyrazosulfuron-ethyl fenchlorazole B-609 pyroxsulam fenchlorazole B-610rimsulfuron fenchlorazole B-611 sulfosulfuron fenchlorazole B-612thiencarbazone-methyl fenchlorazole B-613 tritosulfuron fenchlorazoleB-614 2,4-D and its salts and esters fenchlorazole B-615 aminopyralidand its salts and esters fenchlorazole B-616 clopyralid and its saltsand esters fenchlorazole B-617 dicamba and its salts and estersfenchlorazole B-618 fluroxypyr-meptyl fenchlorazole B-619 quincloracfenchlorazole B-620 quinmerac fenchlorazole B-621 H-9 fenchlorazoleB-622 diflufenzopyr fenchlorazole B-623 diflufenzopyr-sodiumfenchlorazole B-624 clomazone fenchlorazole B-625 diflufenicanfenchlorazole B-626 fluorochloridone fenchlorazole B-627 isoxaflutolfenchlorazole B-628 mesotrione fenchlorazole B-629 picolinafenfenchlorazole B-630 sulcotrione fenchlorazole B-631 tefuryltrionefenchlorazole B-632 tembotrione fenchlorazole B-633 topramezonefenchlorazole B-634 H-7 fenchlorazole B-635 atrazine fenchlorazole B-636diuron fenchlorazole B-637 fluometuron fenchlorazole B-638 hexazinonefenchlorazole B-639 isoproturon fenchlorazole B-640 metribuzinfenchlorazole B-641 propanil fenchlorazole B-642 terbuthylazinefenchlorazole B-643 paraquat dichloride fenchlorazole B-644 flumioxazinfenchlorazole B-645 oxyfluorfen fenchlorazole B-646 saflufenacilfenchlorazole B-647 sulfentrazone fenchlorazole B-648 H-1 fenchlorazoleB-649 H-2 fenchlorazole B-650 glyphosate fenchlorazole B-651glyphosate-isopropylammonium fenchlorazole B-652 glyphosate-trimesium(sulfosate) fenchlorazole B-653 glufosinate fenchlorazole B-654glufosinate-ammonium fenchlorazole B-655 pendimethalin fenchlorazoleB-656 trifluralin fenchlorazole B-657 acetochlor fenchlorazole B-658cafenstrole fenchlorazole B-659 dimethenamid-P fenchlorazole B-660fentrazamide fenchlorazole B-661 flufenacet fenchlorazole B-662mefenacet fenchlorazole B-663 metazachlor fenchlorazole B-664metolachlor-S fenchlorazole B-665 pyroxasulfone fenchlorazole B-666isoxaben fenchlorazole B-667 dymron fenchlorazole B-668 indanofanfenchlorazole B-669 oxaziclomefone fenchlorazole B-670 triaziflamfenchlorazole B-671 atrazine + H-1 fenchlorazole B-672 atrazine +glyphosate fenchlorazole B-673 atrazine + mesotrione fenchlorazole B-674atrazine + nicosulfuron fenchlorazole B-675 atrazine + tembotrionefenchlorazole B-676 atrazine + topramezone fenchlorazole B-677clomazone + glyphosate fenchlorazole B-678 diflufenican +clodinafop-propargyl fenchlorazole B-679 diflufenican +fenoxaprop-P-ethyl fenchlorazole B-680 diflufenican +flupyrsulfuron-methyl-sodium fenchlorazole B-681 diflufenican +glyphosate fenchlorazole B-682 diflufenican + mesosulfuron-methylfenchlorazole B-683 diflufenican + pinoxaden fenchlorazole B-684diflufenican + pyroxsulam fenchlorazole B-685 flumetsulam + glyphosatefenchlorazole B-686 flumioxazin + glyphosate fenchlorazole B-687imazapic + glyphosate fenchlorazole B-688 imazethapyr + glyphosatefenchlorazole B-689 isoxaflutol + H-1 fenchlorazole B-690 isoxaflutol +glyphosate fenchlorazole B-691 metazachlor + H-1 fenchlorazole B-692metazachlor + glyphosate fenchlorazole B-693 metazachlor + mesotrionefenchlorazole B-694 metazachlor + nicosulfuron fenchlorazole B-695metazachlor + terbuthylazine fenchlorazole B-696 metazachlor +topramezone fenchlorazole B-697 metribuzin + glyphosate fenchlorazoleB-698 pendimethalin + H-1 fenchlorazole B-699 pendimethalin +clodinafop-propargyl fenchlorazole B-700 pendimethalin +fenoxaprop-P-ethyl fenchlorazole B-701 pendimethalin +flupyrsulfuron-methyl-sodium fenchlorazole B-702 pendimethalin +glyphosate fenchlorazole B-703 pendimethalin + mesosulfuron-methylfenchlorazole B-704 pendimethalin + mesotrione fenchlorazole B-705pendimethalin + nicosulfuron fenchlorazole B-706 pendimethalin +pinoxaden fenchlorazole B-707 pendimethalin + pyroxsulam fenchlorazoleB-708 pendimethalin + tembotrione fenchlorazole B-709 pendimethalin +topramezone fenchlorazole B-710 pyroxasulfone + tembotrionefenchlorazole B-711 pyroxasulfone + topramezone fenchlorazole B-712sulfentrazone + glyphosate fenchlorazole B-713 terbuthylazine + H-1fenchlorazole B-714 terbuthylazine + foramsulfuron fenchlorazole B-715terbuthylazine + glyphosate fenchlorazole B-716 terbuthylazine +mesotrione fenchlorazole B-717 terbuthylazine + nicosulfuronfenchlorazole B-718 terbuthylazine + tembotrione fenchlorazole B-719terbuthylazine + topramezone fenchlorazole B-720 trifluralin +glyphosate fenchlorazole B-721 clodinafop-propargyl isoxadifen B-722cycloxydim isoxadifen B-723 cyhalofop-butyl isoxadifen B-724fenoxaprop-P-ethyl isoxadifen B-725 pinoxaden isoxadifen B-726profoxydim isoxadifen B-727 tepraloxydim isoxadifen B-728 tralkoxydimisoxadifen B-729 esprocarb isoxadifen B-730 prosulfocarb isoxadifenB-731 thiobencarb isoxadifen B-732 triallate isoxadifen B-733bensulfuron-methyl isoxadifen B-734 bispyribac-sodium isoxadifen B-735cyclosulfamuron isoxadifen B-736 flumetsulam isoxadifen B-737flupyrsulfuron-methyl-sodium isoxadifen B-738 foramsulfuron isoxadifenB-739 imazamox isoxadifen B-740 imazapic isoxadifen B-741 imazapyrisoxadifen B-742 imazaquin isoxadifen B-743 imazethapyr isoxadifen B-744imazosulfuron isoxadifen B-745 iodosulfuron-methyl-sodium isoxadifenB-746 mesosulfuron isoxadifen B-747 nicosulfuron isoxadifen B-748penoxsulam isoxadifen B-749 propoxycarbazone-sodium isoxadifen B-750pyrazosulfuron-ethyl isoxadifen B-751 pyroxsulam isoxadifen B-752rimsulfuron isoxadifen B-753 sulfosulfuron isoxadifen B-754thiencarbazone-methyl isoxadifen B-755 tritosulfuron isoxadifen B-7562,4-D and its salts and esters isoxadifen B-757 aminopyralid and itssalts and esters isoxadifen B-758 clopyralid and its salts and estersisoxadifen B-759 dicamba and its salts and esters isoxadifen B-760fluroxypyr-meptyl isoxadifen B-761 quinclorac isoxadifen B-762 quinmeracisoxadifen B-763 H-9 isoxadifen B-764 diflufenzopyr isoxadifen B-765diflufenzopyr-sodium isoxadifen B-766 clomazone isoxadifen B-767diflufenican isoxadifen B-768 fluorochloridone isoxadifen B-769isoxaflutol isoxadifen B-770 mesotrione isoxadifen B-771 picolinafenisoxadifen B-772 sulcotrione isoxadifen B-773 tefuryltrione isoxadifenB-774 tembotrione isoxadifen B-775 topramezone isoxadifen B-776 H-7isoxadifen B-777 atrazine isoxadifen B-778 diuron isoxadifen B-779fluometuron isoxadifen B-780 hexazinone isoxadifen B-781 isoproturonisoxadifen B-782 metribuzin isoxadifen B-783 propanil isoxadifen B-784terbuthylazine isoxadifen B-785 paraquat dichloride isoxadifen B-786flumioxazin isoxadifen B-787 oxyfluorfen isoxadifen B-788 saflufenacilisoxadifen B-789 sulfentrazone isoxadifen B-790 H-1 isoxadifen B-791 H-2isoxadifen B-792 glyphosate isoxadifen B-793glyphosate-isopropylammonium isoxadifen B-794 glyphosate-trimesium(sulfosate) isoxadifen B-795 glufosinate isoxadifen B-796glufosinate-ammonium isoxadifen B-797 pendimethalin isoxadifen B-798trifluralin isoxadifen B-799 acetochlor isoxadifen B-800 cafenstroleisoxadifen B-801 dimethenamid-P isoxadifen B-802 fentrazamide isoxadifenB-803 flufenacet isoxadifen B-804 mefenacet isoxadifen B-805 metazachlorisoxadifen B-806 metolachlor-S isoxadifen B-807 pyroxasulfone isoxadifenB-808 isoxaben isoxadifen B-809 dymron isoxadifen B-810 indanofanisoxadifen B-811 oxaziclomefone isoxadifen B-812 triaziflam isoxadifenB-813 atrazine + H-1 isoxadifen B-814 atrazine + glyphosate isoxadifenB-815 atrazine + mesotrione isoxadifen B-816 atrazine + nicosulfuronisoxadifen B-817 atrazine + tembotrione isoxadifen B-818 atrazine +topramezone isoxadifen B-819 clomazone + glyphosate isoxadifen B-820diflufenican + clodinafop-propargyl isoxadifen B-821 diflufenican +fenoxaprop-P-ethyl isoxadifen B-822 diflufenican +flupyrsulfuron-methyl-sodium isoxadifen B-823 diflufenican + glyphosateisoxadifen B-824 diflufenican + mesosulfuron-methyl isoxadifen B-825diflufenican + pinoxaden isoxadifen B-826 diflufenican + pyroxsulamisoxadifen B-827 flumetsulam + glyphosate isoxadifen B-828 flumioxazin +glyphosate isoxadifen B-829 imazapic + glyphosate isoxadifen B-830imazethapyr + glyphosate isoxadifen B-831 isoxaflutol + H-1 isoxadifenB-832 isoxaflutol + glyphosate isoxadifen B-833 metazachlor + H-1isoxadifen B-834 metazachlor + glyphosate isoxadifen B-835 metazachlor +mesotrione isoxadifen B-836 metazachlor + nicosulfuron isoxadifen B-837metazachlor + terbuthylazine isoxadifen B-838 metazachlor + topramezoneisoxadifen B-839 metribuzin + glyphosate isoxadifen B-840pendimethalin + H-1 isoxadifen B-841 pendimethalin +clodinafop-propargyl isoxadifen B-842 pendimethalin + fenoxaprop-P-ethylisoxadifen B-843 pendimethalin + flupyrsulfuron-methyl-sodium isoxadifenB-844 pendimethalin + glyphosate isoxadifen B-845 pendimethalin +mesosulfuron-methyl isoxadifen B-846 pendimethalin + mesotrioneisoxadifen B-847 pendimethalin + nicosulfuron isoxadifen B-848pendimethalin + pinoxaden isoxadifen B-849 pendimethalin + pyroxsulamisoxadifen B-850 pendimethalin + tembotrione isoxadifen B-851pendimethalin + topramezone isoxadifen B-852 pyroxasulfone + tembotrioneisoxadifen B-853 pyroxasulfone + topramezone isoxadifen B-854sulfentrazone + glyphosate isoxadifen B-855 terbuthylazine + H-1isoxadifen B-856 terbuthylazine + foramsulfuron isoxadifen B-857terbuthylazine + glyphosate isoxadifen B-858 terbuthylazine + mesotrioneisoxadifen B-859 terbuthylazine + nicosulfuron isoxadifen B-860terbuthylazine + tembotrione isoxadifen B-861 terbuthylazine +topramezone isoxadifen B-862 trifluralin + glyphosate isoxadifen B-863clodinafop-propargyl mefenpyr B-864 cycloxydim mefenpyr B-865cyhalofop-butyl mefenpyr B-866 fenoxaprop-P-ethyl mefenpyr B-867pinoxaden mefenpyr B-868 profoxydim mefenpyr B-869 tepraloxydim mefenpyrB-870 tralkoxydim mefenpyr B-871 esprocarb mefenpyr B-872 prosulfocarbmefenpyr B-873 thiobencarb mefenpyr B-874 triallate mefenpyr B-875bensulfuron-methyl mefenpyr B-876 bispyribac-sodium mefenpyr B-877cyclosulfamuron mefenpyr B-878 flumetsulam mefenpyr B-879flupyrsulfuron-methyl-sodium mefenpyr B-880 foramsulfuron mefenpyr B-881imazamox mefenpyr B-882 imazapic mefenpyr B-883 imazapyr mefenpyr B-884imazaquin mefenpyr B-885 imazethapyr mefenpyr B-886 imazosulfuronmefenpyr B-887 iodosulfuron-methyl-sodium mefenpyr B-888 mesosulfuronmefenpyr B-889 nicosulfuron mefenpyr B-890 penoxsulam mefenpyr B-891propoxycarbazone-sodium mefenpyr B-892 pyrazosulfuron-ethyl mefenpyrB-893 pyroxsulam mefenpyr B-894 rimsulfuron mefenpyr B-895 sulfosulfuronmefenpyr B-896 thiencarbazone-methyl mefenpyr B-897 tritosulfuronmefenpyr B-898 2,4-D and its salts and esters mefenpyr B-899aminopyralid and its salts and esters mefenpyr B-900 clopyralid and itssalts and esters mefenpyr B-901 dicamba and its salts and estersmefenpyr B-902 fluroxypyr-meptyl mefenpyr B-903 quinclorac mefenpyrB-904 quinmerac mefenpyr B-905 H-9 mefenpyr B-906 diflufenzopyr mefenpyrB-907 diflufenzopyr-sodium mefenpyr B-908 clomazone mefenpyr B-909diflufenican mefenpyr B-910 fluorochloridone mefenpyr B-911 isoxaflutolmefenpyr B-912 mesotrione mefenpyr B-913 picolinafen mefenpyr B-914sulcotrione mefenpyr B-915 tefuryltrione mefenpyr B-916 tembotrionemefenpyr B-917 topramezone mefenpyr B-918 H-7 mefenpyr B-919 atrazinemefenpyr B-920 diuron mefenpyr B-921 fluometuron mefenpyr B-922hexazinone mefenpyr B-923 isoproturon mefenpyr B-924 metribuzin mefenpyrB-925 propanil mefenpyr B-926 terbuthylazine mefenpyr B-927 paraquatdichloride mefenpyr B-928 flumioxazin mefenpyr B-929 oxyfluorfenmefenpyr B-930 saflufenacil mefenpyr B-931 sulfentrazone mefenpyr B-932H-1 mefenpyr B-933 H-2 mefenpyr B-934 glyphosate mefenpyr B-935glyphosate-isopropylammonium mefenpyr B-936 glyphosate-trimesium(sulfosate) mefenpyr B-937 glufosinate mefenpyr B-938glufosinate-ammonium mefenpyr B-939 pendimethalin mefenpyr B-940trifluralin mefenpyr B-941 acetochlor mefenpyr B-942 cafenstrolemefenpyr B-943 dimethenamid-P mefenpyr B-944 fentrazamide mefenpyr B-945flufenacet mefenpyr B-946 mefenacet mefenpyr B-947 metazachlor mefenpyrB-948 metolachlor-S mefenpyr B-949 pyroxasulfone mefenpyr B-950 isoxabenmefenpyr B-951 dymron mefenpyr B-952 indanofan mefenpyr B-953oxaziclomefone mefenpyr B-954 triaziflam mefenpyr B-955 atrazine + H-1mefenpyr B-956 atrazine + glyphosate mefenpyr B-957 atrazine +mesotrione mefenpyr B-958 atrazine + nicosulfuron mefenpyr B-959atrazine + tembotrione mefenpyr B-960 atrazine + topramezone mefenpyrB-961 clomazone + glyphosate mefenpyr B-962 diflufenican +clodinafop-propargyl mefenpyr B-963 diflufenican + fenoxaprop-P-ethylmefenpyr B-964 diflufenican + flupyrsulfuron-methyl-sodium mefenpyrB-965 diflufenican + glyphosate mefenpyr B-966 diflufenican +mesosulfuron-methyl mefenpyr B-967 diflufenican + pinoxaden mefenpyrB-968 diflufenican + pyroxsulam mefenpyr B-969 flumetsulam + glyphosatemefenpyr B-970 flumioxazin + glyphosate mefenpyr B-971 imazapic +glyphosate mefenpyr B-972 imazethapyr + glyphosate mefenpyr B-973isoxaflutol + H-1 mefenpyr B-974 isoxaflutol + glyphosate mefenpyr B-975metazachlor + H-1 mefenpyr B-976 metazachlor + glyphosate mefenpyr B-977metazachlor + mesotrione mefenpyr B-978 metazachlor + nicosulfuronmefenpyr B-979 metazachlor + terbuthylazine mefenpyr B-980 metazachlor +topramezone mefenpyr B-981 metribuzin + glyphosate mefenpyr B-982pendimethalin + H-1 mefenpyr B-983 pendimethalin + clodinafop-propargylmefenpyr B-984 pendimethalin + fenoxaprop-P-ethyl mefenpyr B-985pendimethalin + flupyrsulfuron-methyl-sodium mefenpyr B-986pendimethalin + glyphosate mefenpyr B-987 pendimethalin +mesosulfuron-methyl mefenpyr B-988 pendimethalin + mesotrione mefenpyrB-989 pendimethalin + nicosulfuron mefenpyr B-990 pendimethalin +pinoxaden mefenpyr B-991 pendimethalin + pyroxsulam mefenpyr B-992pendimethalin + tembotrione mefenpyr B-993 pendimethalin + topramezonemefenpyr B-994 pyroxasulfone + tembotrione mefenpyr B-995pyroxasulfone + topramezone mefenpyr B-996 sulfentrazone + glyphosatemefenpyr B-997 terbuthylazine + H-1 mefenpyr B-998 terbuthylazine +foramsulfuron mefenpyr B-999 terbuthylazine + glyphosate mefenpyr B-1000terbuthylazine + mesotrione mefenpyr B-1001 terbuthylazine +nicosulfuron mefenpyr B-1002 terbuthylazine + tembotrione mefenpyrB-1003 terbuthylazine + topramezone mefenpyr B-1004 trifluralin +glyphosate mefenpyr B-1005 clodinafop-propargyl H-12 B-1006 cycloxydimH-12 B-1007 cyhalofop-butyl H-12 B-1008 fenoxaprop-P-ethyl H-12 B-1009pinoxaden H-12 B-1010 profoxydim H-12 B-1011 tepraloxydim H-12 B-1012tralkoxydim H-12 B-1013 esprocarb H-12 B-1014 prosulfocarb H-12 B-1015thiobencarb H-12 B-1016 triallate H-12 B-1017 bensulfuron-methyl H-12B-1018 bispyribac-sodium H-12 B-1019 cyclosulfamuron H-12 B-1020flumetsulam H-12 B-1021 flupyrsulfuron-methyl-sodium H-12 B-1022foramsulfuron H-12 B-1023 imazamox H-12 B-1024 imazapic H-12 B-1025imazapyr H-12 B-1026 imazaquin H-12 B-1027 imazethapyr H-12 B-1028imazosulfuron H-12 B-1029 iodosulfuron-methyl-sodium H-12 B-1030mesosulfuron H-12 B-1031 nicosulfuron H-12 B-1032 penoxsulam H-12 B-1033propoxycarbazone-sodium H-12 B-1034 pyrazosulfuron-ethyl H-12 B-1035pyroxsulam H-12 B-1036 rimsulfuron H-12 B-1037 sulfosulfuron H-12 B-1038thiencarbazone-methyl H-12 B-1039 tritosulfuron H-12 B-1040 2,4-D andits salts and esters H-12 B-1041 aminopyralid and its salts and estersH-12 B-1042 clopyralid and its salts and esters H-12 B-1043 dicamba andits salts and esters H-12 B-1044 fluroxypyr-meptyl H-12 B-1045quinclorac H-12 B-1046 quinmerac H-12 B-1047 B-9 H-12 B-1048diflufenzopyr H-12 B-1049 diflufenzopyr-sodium H-12 B-1050 clomazoneH-12 B-1051 diflufenican H-12 B-1052 fluorochloridone H-12 B-1053isoxaflutol H-12 B-1054 mesotrione H-12 B-1055 picolinafen H-12 B-1056sulcotrione H-12 B-1057 tefuryltrione H-12 B-1058 tembotrione H-12B-1059 topramezone H-12 B-1060 H-7 H-12 B-1061 atrazine H-12 B-1062diuron H-12 B-1063 fluometuron H-12 B-1064 hexazinone H-12 B-1065isoproturon H-12 B-1066 metribuzin H-12 B-1067 propanil H-12 B-1068terbuthylazine H-12 B-1069 paraquat dichloride H-12 B-1070 flumioxazinH-12 B-1071 oxyfluorfen H-12 B-1072 saflufenacil H-12 B-1073sulfentrazone H-12 B-1074 H-1 H-12 B-1075 H-2 H-12 B-1076 glyphosateH-12 B-1077 glyphosate-isopropylammonium H-12 B-1078glyphosate-trimesium (sulfosate) H-12 B-1079 glufosinate H-12 B-1080glufosinate-ammonium H-12 B-1081 pendimethalin H-12 B-1082 trifluralinH-12 B-1083 acetochlor H-12 B-1084 cafenstrole H-12 B-1085dimethenamid-P H-12 B-1086 fentrazamide H-12 B-1087 flufenacet H-12B-1088 mefenacet H-12 B-1089 metazachlor H-12 B-1090 metolachlor-S H-12B-1091 pyroxasulfone H-12 B-1092 isoxaben H-12 B-1093 dymron H-12 B-1094indanofan H-12 B-1095 oxaziclomefone H-12 B-1096 triaziflam H-12 B-1097atrazine + H-1 H-12 B-1098 atrazine + glyphosate H-12 B-1099 atrazine +mesotrione H-12 B-1100 atrazine + nicosulfuron H-12 B-1101 atrazine +tembotrione H-12 B-1102 atrazine + topramezone H-12 B-1103 clomazone +glyphosate H-12 B-1104 diflufenican + clodinafop-propargyl H-12 B-1105diflufenican + fenoxaprop-P-ethyl H-12 B-1106 diflufenican +flupyrsulfuron-methyl-sodium H-12 B-1107 diflufenican + glyphosate H-12B-1108 diflufenican + mesosulfuron-methyl H-12 B-1109 diflufenican +pinoxaden H-12 B-1110 diflufenican + pyroxsulam H-12 B-1111flumetsulam + glyphosate H-12 B-1112 flumioxazin + glyphosate H-12B-1113 imazapic + glyphosate H-12 B-1114 imazethapyr + glyphosate H-12B-1115 isoxaflutol + H-1 H-12 B-1116 isoxaflutol + glyphosate H-12B-1117 metazachlor + H-1 H-12 B-1118 metazachlor + glyphosate H-12B-1119 metazachlor + mesotrione H-12 B-1120 metazachlor + nicosulfuronH-12 B-1121 metazachlor + terbuthylazine H-12 B-1122 metazachlor +topramezone H-12 B-1123 metribuzin + glyphosate H-12 B-1124pendimethalin + H-1 H-12 B-1125 pendimethalin + clodinafop-propargylH-12 B-1126 pendimethalin + fenoxaprop-P-ethyl H-12 B-1127pendimethalin + flupyrsulfuron-methyl-sodium H-12 B-1128 pendimethalin +glyphosate H-12 B-1129 pendimethalin + mesosulfuron-methyl H-12 B-1130pendimethalin + mesotrione H-12 B-1131 pendimethalin + nicosulfuron H-12B-1132 pendimethalin + pinoxaden H-12 B-1133 pendimethalin + pyroxsulamH-12 B-1134 pendimethalin + tembotrione H-12 B-1135 pendimethalin +topramezone H-12 B-1136 pyroxasulfone + tembotrione H-12 B-1137pyroxasulfone + topramezone H-12 B-1138 sulfentrazone + glyphosate H-12B-1139 terbuthylazine + H-1 H-12 B-1140 terbuthylazine + foramsulfuronH-12 B-1141 terbuthylazine + glyphosate H-12 B-1142 terbuthylazine +mesotrione H-12 B-1143 terbuthylazine + nicosulfuron H-12 B-1144terbuthylazine + tembotrione H-12 B-1145 terbuthylazine + topramezoneH-12 B-1146 trifluralin + glyphosate H-12 B-1147 2-1 — B-1148 2-2 —B-1149 2-3 — B-1150 2-4 — B-1151 2-5 — B-1152 2-6 — B-1153 2-7 — B-11542-8 — B-1155 2-9 — B-1156 2-1 benoxacor B-1157 2-2 benoxacor B-1158 2-3benoxacor B-1159 2-4 benoxacor B-1160 2-5 benoxacor B-1161 2-6 benoxacorB-1162 2-7 benoxacor B-1163 2-8 benoxacor B-1164 2-9 benoxacor B-11652-1 cloquintocet B-1166 2-2 cloquintocet B-1167 2-3 cloquintocet B-11682-4 cloquintocet B-1169 2-5 cloquintocet B-1170 2-6 cloquintocet B-11712-7 cloquintocet B-1172 2-8 cloquintocet B-1173 2-9 cloquintocet B-11742-1 cyprosulfamide B-1175 2-2 cyprosulfamide B-1176 2-3 cyprosulfamideB-1177 2-4 cyprosulfamide B-1178 2-5 cyprosulfamide B-1179 2-6cyprosulfamide B-1180 2-7 cyprosulfamide B-1181 2-8 cyprosulfamideB-1182 2-9 cyprosulfamide B-1183 2-1 dichlormid B-1184 2-2 dichlormidB-1185 2-3 dichlormid B-1186 2-4 dichlormid B-1187 2-5 dichlormid B-11882-6 dichlormid B-1189 2-7 dichlormid B-1190 2-8 dichlormid B-1191 2-9dichlormid B-1192 2-1 fenchlorazole B-1193 2-2 fenchlorazole B-1194 2-3fenchlorazole B-1195 2-4 fenchlorazole B-1196 2-5 fenchlorazole B-11972-6 fenchlorazole B-1198 2-7 fenchlorazole B-1199 2-8 fenchlorazoleB-1200 2-9 fenchlorazole B-1201 2-1 isoxadifen B-1202 2-2 isoxadifenB-1203 2-3 isoxadifen B-1204 2-4 isoxadifen B-1205 2-5 isoxadifen B-12062-6 isoxadifen B-1207 2-7 isoxadifen B-1208 2-8 isoxadifen B-1209 2-9isoxadifen B-1210 2-1 mefenpyr B-1211 2-2 mefenpyr B-1212 2-3 mefenpyrB-1213 2-4 mefenpyr B-1214 2-5 mefenpyr B-1215 2-6 mefenpyr B-1216 2-7mefenpyr B-1217 2-8 mefenpyr B-1218 2-9 mefenpyr B-1219 2-1 H-11 B-12202-2 H-11 B-1221 2-3 H-11 B-1222 2-4 H-11 B-1223 2-5 H-11 B-1224 2-6 H-11B-1225 2-7 H-11 B-1226 2-8 H-11 B-1227 2-9 H-11 B-1228 2-1 H-12 B-12292-2 H-12 B-1230 2-3 H-12 B-1231 2-4 H-12 B-1232 2-5 H-12 B-1233 2-6 H-12B-1234 2-7 H-12 B-1235 2-8 H-12 B-1236 2-9 H-12

The compounds of formula I and the compositions according to theinvention may also have a plant-strengthening action. Accordingly, theyare suitable for mobilizing the defense system of the plants againstattack by unwanted microorganisms, such as harmful fungi, but alsoviruses and bacteria. Plant-strengthening (resistance-inducing)substances are to be understood as meaning, in the present context,those substances which are capable of stimulating the defense system oftreated plants in such a way that, when subsequently inoculated byunwanted microorganisms, the treated plants display a substantial degreeof resistance to these microorganisms.

The compounds of formula I can be employed for protecting plants againstattack by unwanted microorganisms within a certain period of time afterthe treatment. The period of time within which their protection iseffected generally extends from 1 to 28 days, preferably from 1 to 14days, after the treatment of the plants with the compounds of formula I,or, after treatment of the seed, for up to 9 months after sowing.

The compounds of formula I and the compositions according to theinvention are also suitable for increasing the harvest yield.

Moreover, they have reduced toxicity and are tolerated well by theplants.

1-31. (canceled)
 32. A compound of formula I,

an N-oxide or an agriculturally suitable salt thereof, wherein R¹ isselected from the group consisting of halogen, C₁-C₈-alkyl,C₁-C₈-haloalkyl, nitro, C₁-C₄-alkoxy-C₁-C₄-alkyl, cyano-Z¹,C₂-C₅-alkenyl, C₂-C₅-alkynyl, C₃-C₁₀-cycloalkyl-Z¹, C₂-C₅-haloalkenyl,C₃-C₅-haloalkynyl, C₁-C₈-alkoxy, C₁-C₄-alkoxy-C₁-C₄-alkoxy-Z¹,C₁-C₄-alkylthio-C₁-C₄-alkyl, C₁-C₄-alkylthio-C₁-C₄-alkylthio-Z¹,C₂-C₆-alkenyloxy, C₂-C₆-alkynyloxy, C₁-C₆-haloalkoxy,C₁-C₄-haloalkoxy-C₁-C₄-alkyl, C₁-C₄-haloalkoxy-C₁-C₄-alkoxy-Z¹,R^(1b)—S(O)_(k)—Z¹, phenoxy-Z¹ and heterocyclyloxy-Z¹, whereheterocyclyloxy is an oxygen bound 5- or 6-membered monocyclic or 8-, 9-or 10-membered bicyclic saturated, partially unsaturated or aromaticheterocycle, which contains 1, 2, 3 or 4 heteroatoms as ring members,which are selected from the group consisting of O, N and S, where thecyclic groups in phenoxy and heterocyclyloxy are unsubstituted orsubstituted by 1, 2, 3 or 4 groups R¹¹, which are identical ordifferent; X is N or CR²; R² is selected from the group consisting ofhydrogen, halogen, hydroxy-Z², nitro, C₁-C₄-nitroalkyl, cyano,C₁-C₄-cyanoalkyl, C₁-C₆-alkyl, C₂-C₅-alkenyl, C₂-C₈-alkynyl,C₃-C₁₀-cycloalkyl-Z², C₃-C₁₀-cycloalkoxy-Z², where the C₃-C₁₀-cycloalkylgroups in the two aforementioned radicals are unsubstituted or partiallyor completely halogenated, C₁-C₅-haloalkyl, C₂-C₅-haloalkenyl,C₃-C₅-haloalkynyl, C₁-C₅-alkoxy-Z², C₁-C₅-haloalkoxy-Z²,C₃-C₁₀-cycloalkyl-C₁-C₂-alkoxy, C₁-C₄-alkoxy-C₁-C₄-alkoxy-Z²,C₁-C₄-alkylthio-C₁-C₄-alkylthio-Z², C₂-C₈-alkenyloxy-Z²,C₂-C₅-alkynyloxy-Z², C₂-C₅-haloalkenyloxy-Z², C₃-C₅-haloalkynyloxy-Z²,C₁-C₄-haloalkoxy-C₁-C₄-alkoxy-Z², (tri-C₁-C₄-alkyl)silyl-Z²,R^(2b)—S(O)_(k)-Z², R^(2c)—C(═O)—Z², R^(2d)O—C(═O)—Z, R^(2d)O—N═CH—Z²,R^(2d)O—N═CC₁-C₄-alkyl-Z², R^(2d)O—N═CC₁-C₄-haloalkyl-Z²,R^(2c)R^(2d)C═N—O—C₁-C₄-alkyl, R^(2e)R^(2f)N—C(═O)—Z², R^(2g)R^(2h)N—Z²,phenyl-Z^(2a), heterocyclyl-Z^(2a), where heterocyclyl is a 3-, 4-, 5-or 6-membered monocyclic or 8-, 9- or 10-membered bicyclic saturated,partially unsaturated or aromatic heterocycle, which contains 1, 2, 3 or4 heteroatoms as ring members, which are selected from the groupconsisting of O, N and S, where the cyclic groups in phenyl-Z^(2a) andheterocyclyl-Z^(2a) are unsubstituted or substituted by 1, 2, 3 or 4groups R²¹, which are identical or different, rhodano,C₃-C₆-cycloalkenyl, OC(O)OR²², OC(O)N(R²²)₂, ONC(R²³)₂, OSO₂R²⁵,SO₂OR²², SO₂N(R²²)₂, N(R²²)C(O)OR²², N(R²²)C(O)N(R²²)₂, C(O)N(R²²)OR²,P(O)(O—C₁-C₄-alkyl)₂, C₁-C₆-alkyl-OC(O)R²², C₁-C₆-alkyl-OSO₂R²⁵,C₁-C₆-alkyl-SO₂OR²², C₁-C₆-alkyl-SO₂N(R²²)₂,C₁-C₆-alkyl-P(O)(O—C₁-C₄-alkyl)₂,

R³ is selected from the group consisting of hydrogen, halogen,hydroxy-Z², nitro, C₁-C₄-nitroalkyl, cyano, C₁-C₄-cyanoalkyl,C₁-C₆-alkyl, C₂-C₅-alkenyl, C₂-C₅-alkynyl, C₃-C₁₀-cycloalkyl-Z²,C₃-C₁₀-cycloalkoxy-Z², where the C₃-C₁₀-cycloalkyl groups in the twoaforementioned radicals are unsubstituted or partially or completelyhalogenated, C₁-C₈-haloalkyl, C₂-C₅-haloalkenyl, C₃-C₅-haloalkynyl,C₁-C₈-alkoxy-Z², C₁-C₈-haloalkoxy-Z², C₃-C₁₀-cycloalkyl-C₁-C₂-alkoxy,C₁-C₄-alkoxy-C₁-C₄-alkoxy-Z², C₁-C₄-alkylthio-C₁-C₄-alkylthio-Z²,C₂-C₈-alkenyloxy-Z², C₂-C₅-alkynyloxy-Z², C₂-C₅-haloalkenyloxy-Z²,C₃-C₅-haloalkynyloxy-Z², C₁-C₄-haloalkoxy-C₁-C₄-alkoxy-Z²,(tri-C₁-C₄-alkyl)silyl-Z², R^(2b)—S(O)_(k)-Z², R^(2c)—C(═O)—Z²,R^(2d)O—C(═O)—Z², R^(2d)O—N═CH—Z², R^(2c)R^(2d)C═N—O—C₁-C₄-alkyl,R^(2e)R^(2f)N—C(═O)—Z², R^(2g)R²N—Z², phenyl-Z^(2a),heterocyclyl-Z^(2a), where heterocyclyl is a 3-, 4-, 5- or 6-memberedmonocyclic or 8-, 9- or 10-membered bicyclic saturated, partiallyunsaturated or aromatic heterocycle, which contains 1, 2, 3 or 4heteroatoms as ring members, which are selected from the groupconsisting of O, N and S, where the cyclic groups in phenyl-Z^(2a) andheterocyclyl-Z^(2a) are unsubstituted or substituted by 1, 2, 3 or 4groups R²¹, which are identical or different, rhodano,C₃-C₆-cycloalkenyl, C₃-C₆-halocycloalkenyl,C₃-C₆-cycloalkenyl-C₁-C₆-alkyl, C₃-C₆-halocycloalkenyl-C₁-C₆-alkyl,OC(O)R²², OC(O)OR²⁵, OC(O)N(R²²)₂, OSO₂R²⁵, SO₂OR²², SO₂N(R²²)₂,SO₂N(R²²)C(O)R²², SO₂N(R²²)C(O)OR²⁵, SO₂N(R²²)C(O)N(R²²)₂,N(R²²)C(O)OR²⁵, N(R²²)C(O)N(R²²)₂, N(R²²)S(O)₂OR²², N(R²²)S(O)₂N(R²²)₂,C(O)N(R²²) OR², C(O)N(R²²)N(R²²)₂, C(O)N(R²²)C(O)R²²,C(O)N(R²²)C(O)OR²⁵, C(O)N(R²²)C(O)N(R²²)₂, C(O)N(R²²)SO₂R²⁵,C(O)N(R²²)SO₂OR²², C(O)N(R²²)SO₂N(R²²)₂, P(O)(OH)₂,P(O)(O—C₁-C₄-alkyl)₂, C₁-C₆-alkyl-OC(O)R²², C₁-C₆-alkyl-OC(O)OR²⁵,C₁-C₆-alkyl-OC(O)N(R²²)₂, C₁-C₆-alkyl-OSO₂R²⁵, C₁-C₆-alkyl-SO₂OR²²,C₁-C₆-alkyl-SO₂N(R²²)₂, C₁-C₆-alkyl-SO₂N(R²²)C(O)R²²,C₁-C₆-alkyl-SO₂N(R²²)C(O)OR²⁵, C₁-C₆-alkyl-SO₂N(R²²)C(O)N(R²²)₂,C₁-C₆-alkyl-N(R²²)C(O)OR²⁵, C₁-C₆-alkyl-N(R²²)C(O)N(R²²)₂,C₁-C₆-alkyl-N(R²²)S(O)₂OR²², C₁-C₆-alkyl-N(R²²)S(O)₂N(R²²)₂,C₁-C₆-alkyl-C(O)N(R²²)OR²², C₁-C₆-alkyl-C(O)N(R²²)N(R²²)₂,C₁-C₆-alkyl-C(O)N(R²²)C(O)R²², C₁-C₆-alkyl-C(O)N(R²²)C(O)OR²⁵,C₁-C₆-alkyl-C(O)N(R²²)C(O)N(R²²)₂, C₁-C₆-alkyl-C(O)N(R²²)SO₂R²⁵,C₁-C₆-alkyl-C(O)N(R²²)SO₂OR²², C₁-C₆-alkyl-C(O)N(R²²)SO₂N(R²²)₂,C₁-C₆-alkyl-P(O)(OH)₂ and C₁-C₆-alkyl-P(O)(O—C₁-C₄-alkyl)₂; R⁴ isselected from the group consisting of hydrogen, halogen, C₁-C₈-alkyl,cyano-Z¹, nitro, C₃-C₇-cycloalkyl, C₃-C₇-cycloalkyl-C₁-C₄-alkyl, wherethe C₃-C₇-cycloalkyl groups in the two aforementioned radicals areunsubstituted or partially or completely halogenated, C₂-C₅-alkenyl,C₂-C₅-alkynyl, C₁-C₈-haloalkyl, C₁-C₃-alkylamino, C₁-C₃-dialkylamino,C₁-C₃-alkylamino-S(O)_(k), C₁-C₃-alkylcarbonyl, C₁-C₈-alkoxy,C₁-C₄-alkoxy-C₁-C₄-alkyl, C₁-C₄-alkoxy-C₁-C₄-alkoxy-Z¹,C₁-C₄-alkylthio-C₁-C₄-alkyl, C₁-C₄-alkylthio-C₁-C₄-alkylthio-Z¹,C₂-C₆-alkenyloxy, C₂-C₆-alkynyloxy, C₁-C₆-haloalkoxy,C₁-C₄-haloalkoxy-C₁-C₄-alkyl, C₁-C₄-haloalkoxy-C₁-C₄-alkoxy-Z¹,R^(1b)—S(O)_(k)—Z¹, phenoxy-Z¹ and heterocyclyloxy-Z¹, whereheterocyclyloxy is an oxygen bound 5- or 6-membered monocyclic or 8-, 9-or 10-membered bicyclic saturated, partially unsaturated or aromaticheterocycle, which contains 1, 2, 3 or 4 heteroatoms as ring members,which are selected from the group consisting of O, N and S, where thecyclic groups in phenoxy and heterocyclyloxy are unsubstituted orsubstituted by 1, 2, 3 or 4 groups R¹¹, which are identical ordifferent; R⁵ is selected from the group consisting of halogen,cyano-Z¹, nitro, C₁-C₅-alkyl, C₃-C₇-cycloalkyl,C₃-C₇-cycloalkyl-C₁-C₄-alkyl, where the C₃-C₇-cycloalkyl groups in thetwo aforementioned radicals are unsubstituted or partially or completelyhalogenated, C₂-C₅-alkenyl, C₂-C₅-alkynyl, C₁-C₈-haloalkyl,C₁-C₃-alkylamino, C₁-C₃-dialkylamino, C₁-C₃-alkylamino-S(O)_(k),C₁-C₃-alkylcarbonyl, C₁-C₅-alkoxy, C₁-C₄-alkoxy-C₁-C₄-alkyl,C₁-C₄-alkoxy-C₁-C₄-alkoxy-Z¹, C₁-C₄-alkylthio-C₁-C₄-alkyl,C₁-C₄-alkylthio-C₁-C₄-alkylthio-Z¹, C₂-C₆-alkenyloxy, C₂-C₆-alkynyloxy,C₁-C₆-haloalkoxy, C₁-C₄-haloalkoxy-C₁-C₄-alkyl,C₁-C₄-haloalkoxy-C₁-C₄-alkoxy-Z¹, R^(1b)—S(O)_(k)—Z¹, phenoxy-Z¹ andheterocyclyloxy-Z¹, where heterocyclyloxy is an oxygen bound 5- or6-membered monocyclic or 8-, 9- or 10-membered bicyclic saturated,partially unsaturated or aromatic heterocycle, which contains 1, 2, 3 or4 heteroatoms as ring members, which are selected from the groupconsisting of O, N and S, where the cyclic groups in phenoxy andheterocyclyloxy are unsubstituted or substituted by 1, 2, 3 or 4 groupsR¹¹, which are identical or different; R⁶ is selected from the groupconsisting of cyano, nitro, hydroxy, amino, C₁-C₆-alkyl,C₁-C₆-cyano-alkyl, C₃-C₇-cycloalkyl, C₃-C₇-cycloalkyl-C₁-C₄-alkyl, wherethe C₃-C₇-cycloalkyl groups in the two aforementioned radicals areunsubstituted or partially or completely halogenated, C₁-C₆-haloalkyl,C₁-C₆-alkoxy, C₁-C₆-alkylcarbonyl, C₁-C₆-alkyaminocarbonyl,C₁-C₆-dialkyl-aminocarbonyl, C₁-C₆-alkyamino, C₁-C₆-dialkyl-amino,C₂-C₆-alkenyl, C₂-C₆-haloalkenyl, C₂-C₆-alkynyl, C₂-C₆-haloalkynyl,C₁-C₄-alkoxy-C₁-C₄-alkyl, C₁-C₄-haloalkoxy-C₁-C₄-alkyl,R^(b)R^(b)N—S(O)_(n)—Z, R^(b)O—S(O)_(n)—Z, R^(b)—S(O)_(n)—Z,R^(c)R^(c)N—C₁-C₃-alkyl-S(O)_(n)—C₁-C₃-alkyl, R^(c)—C(═O)—C₁-C₃-alkyl,R^(d)—C(═O)O—C₁-C₃-alkyl, R^(d)—O—C(═O)O—C₁-C₃-alkyl,R^(d)O—C(═O)—C₁-C₃-alkyl, R^(e)R^(f)N—C(═O)—C₁-C₃-alkyl,R^(c)—C(═O)R^(e)N—C₁-C₃-alkyl, R^(b)—S(O)_(n)—R^(e)N—C₁-C₃-alkyl,R^(c)R^(c)N—C₁-C₃-alkyl, phenyl-Z and heterocyclyl-Z, where heterocyclylis a 5- or 6-membered monocyclic or 8-, 9- or 10-membered bicyclicsaturated, partially unsaturated or aromatic heterocycle, which contains1, 2, 3 or 4 heteroatoms as ring members, which are selected from thegroup consisting of O, N and S, where phenyl and heterocyclyl areunsubstituted or substituted by 1, 2, 3 or 4 groups R′, which areidentical or different; R⁷ is selected from the group consisting ofhydrogen, C₁-C₆-alkyl, C₃-C₇-cycloalkyl, C₃-C₇-cycloalkyl-C₁-C₄-alkyl,where the C₃-C₇-cycloalkyl groups in the two aforementioned radicals areunsubstituted or partially or completely halogenated, C₁-C₆-haloalkyl,C₂-C₆-alkenyl, C₂-C₆-haloalkenyl, C₂-C₆-alkynyl, C₂-C₆-haloalkynyl,C₁-C₄-alkoxy-C₁-C₄-alkyl, C₁-C₄-haloalkoxy-C₁-C₄-alkyl,R^(b)—S(O)_(n)—C₁-C₃-alkyl, R^(c)—C(═O)—C₁-C₃-alkyl,R^(d)O—C(═O)—C₁-C₃-alkyl, R^(e)R^(f)N—C(═O)—C₁-C₃-alkyl,R^(g)R^(h)N—C₁-C₃-alkyl, phenyl-Z and heterocyclyl-Z, where heterocyclylis a 5- or 6-membered monocyclic or 8-, 9- or 10-membered bicyclicsaturated, partially unsaturated or aromatic heterocycle, which contains1, 2, 3 or 4 heteroatoms as ring members, which are selected from thegroup consisting of O, N and S, where phenyl and heterocyclyl areunsubstituted or substituted by 1, 2, 3 or 4 groups R′, which areidentical or different; B is N or CH; R′, R¹¹, R²¹ independently of eachother are selected from the group consisting of halogen, NO₂, CN,C₁-C₆-alkyl, C₃-C₇-cycloalkyl, C₃-C₇-halocycloalkyl, C₁-C₆-haloalkyl,C₂-C₆-alkenyl, C₂-C₆-haloalkenyl, C₂-C₆-alkynyl, C₂-C₆-haloalkynyl,C₁-C₆-alkoxy, C₁-C₄-alkoxy-C₁-C₄-alkyl, C₁-C₄-alkylthio-C₁-C₄-alkyl,C₁-C₄-haloalkoxy-C₁-C₄-alkyl, C₁-C₄-alkoxy-C₁-C₄-alkoxy,C₃-C₇-cycloalkoxy and C₁-C₆-haloalkyloxy, or two vicinal radicals R′,R¹¹ or R²¹ together may form a group ═O; Z, Z¹, Z² independently of eachother are selected from the group consisting of a covalent bond andC₁-C₄-alkanediyl; Z^(2a) is s Z^(2a) selected from the group consistingof a covalent bond, C₁-C₄-alkanediyl, O—C₁-C₄-alkanediyl,C₁-C₄-alkanediyl-O and C₁-C₄-alkanediyl-O—C₁-C₄-alkanediyl; R^(b),R^(1b), R^(2b) independently of each other are selected from the groupconsisting of C₁-C₆-alkyl, C₃-C₇-cycloalkyl, C₁-C₆-haloalkyl,C₂-C₆-alkenyl, C₂-C₆-haloalkenyl, C₂-C₆-alkynyl, C₂-C₆-haloalkynyl,phenyl and heterocyclyl, where heterocyclyl is a 5- or 6-memberedmonocyclic saturated, partially unsaturated or aromatic heterocycle,which contains 1, 2, 3 or 4 heteroatoms as ring members, which areselected from the group consisting of O, N and S, where phenyl andheterocyclyl are unsubstituted or substituted by 1, 2, 3 or 4 groups,which are identical or different and selected from the group consistingof halogen, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy andC₁-C₄-haloalkoxy; R^(c), R^(2c) independently of each other are selectedfrom the group consisting of hydrogen, C₁-C₆-alkyl, C₃-C₇-cycloalkyl,C₃-C₇-cycloalkyl-C₁-C₄-alkyl, where the C₃-C₇-cycloalkyl groups in thetwo aforementioned radicals are unsubstituted or partially or completelyhalogenated, C₁-C₆-haloalkyl, C₂-C₆-alkenyl, C₂-C₆-haloalkenyl,C₂-C₆-alkynyl, C₂-C₆-haloalkynyl, C₁-C₄-alkoxy-C₁-C₄-alkyl, phenyl,benzyl and heterocyclyl, where heterocyclyl is a 5- or 6-memberedmonocyclic saturated, partially unsaturated or aromatic heterocycle,which contains 1, 2, 3 or 4 heteroatoms as ring members, which areselected from the group consisting of O, N and S, where phenyl, benzyland heterocyclyl are unsubstituted or substituted by 1, 2, 3 or 4groups, which are identical or different and selected from the groupconsisting of halogen, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy andC₁-C₄-haloalkoxy; R^(d), R^(2d) independently of each other are selectedfrom the group consisting of C₁-C₆-alkyl, C₃-C₇-cycloalkyl,C₃-C₇-cycloalkyl-C₁-C₄-alkyl, where the C₃-C₇-cycloalkyl groups in thetwo aforementioned radicals are unsubstituted or partially or completelyhalogenated, C₁-C₆-haloalkyl, C₂-C₆-alkenyl, C₂-C₆-haloalkenyl,C₂-C₆-alkynyl, C₂-C₆-haloalkynyl, C₁-C₄-alkoxy-C₁-C₄-alkyl, phenyl andbenzyl, where phenyl and benzyl are unsubstituted or substituted by 1,2, 3 or 4 groups, which are identical or different and selected from thegroup consisting of halogen, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxyand C₁-C₄-haloalkoxy; R^(e), R^(f) independently of each other areselected from the group consisting of hydrogen, C₁-C₆-alkyl,C₃-C₇-cycloalkyl, C₃-C₇-cycloalkyl-C₁-C₄-alkyl, where theC₃-C₇-cycloalkyl groups in the two aforementioned radicals areunsubstituted or partially or completely halogenated, C₁-C₆-haloalkyl,C₂-C₆-alkenyl, C₂-C₆-haloalkenyl, C₂-C₆-alkynyl, C₂-C₆-haloalkynyl,C₁-C₄-alkoxy-C₁-C₄-alkyl, phenyl and benzyl, where phenyl and benzyl areunsubstituted or substituted by 1, 2, 3 or 4 groups, which are identicalor different and selected from the group consisting of halogen,C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy and C₁-C₄-haloalkoxy, orR^(e), R^(f) together with the nitrogen atom, to which they are boundmay form a 5-, 6 or 7-membered, saturated or unsaturated N-boundheterocyclic radical, which may carry as a ring member a furtherheteroatom selected from the group consisting of O, S and N and which isunsubstituted or may carry 1, 2, 3 or 4 groups, which are identical ordifferent and selected from the group consisting of halogen,C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy and C₁-C₄-haloalkoxy; R^(2e),R^(2f) independently of each other have the meanings given for R^(e),R^(f); R^(g) is selected from the group consisting of hydrogen,C₁-C₆-alkyl, C₃-C₇-cycloalkyl, C₃-C₇-cycloalkyl-C₁-C₄-alkyl, where theC₃-C₇-cycloalkyl groups in the two aforementioned radicals areunsubstituted or partially or completely halogenated, C₁-C₆-haloalkyl,C₂-C₆-alkenyl, C₂-C₆-haloalkenyl, C₂-C₆-alkynyl, C₂-C₆-haloalkynyl,C₁-C₄-alkoxy-C₁-C₄-alkyl, C₁-C₄-alkylsulfonyl, C₁-C₄-alkylcarbonyl,phenyl and benzyl, where phenyl and benzyl are unsubstituted orsubstituted by 1, 2, 3 or 4 groups, which are identical or different andselected from the group consisting of halogen, C₁-C₄-alkyl,C₁-C₄-haloalkyl, C₁-C₄-alkoxy and C₁-C₄-haloalkoxy; R^(h) is selectedfrom the group consisting of hydrogen, C₁-C₆-alkyl, C₃-C₇-cycloalkyl,C₃-C₇-cycloalkyl-C₁-C₄-alkyl, where the C₃-C₇-cycloalkyl groups in thetwo aforementioned radicals are unsubstituted or partially or completelyhalogenated, C₁-C₆-haloalkyl, C₂-C₆-alkenyl, C₂-C₆-haloalkenyl,C₂-C₆-alkynyl, C₂-C₆-haloalkynyl, C₁-C₄-alkoxy-C₁-C₄-alkyl,C₁-C₄-alkylsulfonyl, C₁-C₄-alkylcarbonyl, a radical C(═O)—R^(k), phenyland benzyl, where phenyl and benzyl are unsubstituted or substituted by1, 2, 3 or 4 groups, which are identical or different and selected fromthe group consisting of halogen, C₁-C₄-alkyl, C₁-C₄-haloalkyl,C₁-C₄-alkoxy and C₁-C₄-haloalkoxy, or R^(g), R^(h) together with thenitrogen atom, to which they are bound may form a 5-, 6 or 7-membered,saturated or unsaturated N-bound heterocyclic radical, which may carryas a ring member a further heteroatom selected from the group consistingof O, S and N and which is unsubstituted or may carry 1, 2, 3 or 4groups, which are identical or different and selected from the groupconsisting of ═O, halogen, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxyand C₁-C₄-haloalkoxy; R^(2g), R^(2h) independently of each other havethe meanings given for R^(g), R^(h); R^(k) has the meanings given forR^(c); R²² is selected from the group consisting of hydrogen,C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₂-C₆-alkenyl, C₂-C₆-haloalkenyl,C₂-C₆-alkynyl, C₃-C₆-haloalkynyl, C₃-C₆-cycloalkyl, C₃-C₆-cycloalkenyl,C₃-C₆-halocycloalkyl, C₃-C₆-cycloalkyl-C₁-C₆-alkyl,C₁-C₆-alkoxy-C₁-C₆-alkyl, C₃-C₆-cycloalkyl-C₁-C₆-alkoxy-C₁-C₆-alkyl,phenyl, phenyl-C₁-C₆-alkyl, heteroaryl, heteroaryl-C₁-C₆-alkyl,heterocyclyl, heterocyclyl-C₁-C₆-alkyl, phenyl-O—C₁-C₆-alkyl,heteroaryl-O—C₁-C₆-alkyl, heterocyclyl-O—C₁-C₆-alkyl,phenyl-N(R²³)—C₁-C₆-alkyl, heteroaryl-N(R²³)—C₁-C₆-alkyl,heterocyclyl-N(R²³)—C₁-C₆-alkyl, phenyl-S(O)_(n)—C₁-C₆-alkyl,heteroaryl-S(O)_(n)—C₁-C₆-alkyl, heterocyclyl-S(O)_(n)—C₁-C₆-alkyl,where the 15 aforementioned radicals are substituted by s residuesselected from the group consisting of nitro, halogen, cyano, rhodano,C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₃-C₆-cycloalkyl, C(O)OR²³, C(O)N(R²³)₂,OR²³, N(R²³)₂, S(O)_(n)R²⁴, S(O)₂OR²³, S(O)₂N(R²³)₂ andR²³O—C₁-C₆-alkyl, and where heterocyclyl bears 0, 1 or 2 oxo groups; R²³is selected from the group consisting of hydrogen, C₁-C₆-alkyl,C₁-C₆-haloalkyl, C₂-C₆-alkenyl, C₂-C₆-alkynyl, C₃-C₆-cycloalkyl,C₃-C₆-cycloalkyl-C₁-C₆-alkyl and phenyl; R²⁴ is selected from the groupconsisting of C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₂-C₆-alkenyl,C₂-C₆-alkynyl, C₃-C₆-cycloalkyl, C₃-C₆-cycloalkyl-C₁-C₆-alkyl andphenyl; R²⁵ is selected from the group consisting of C₁-C₆-alkyl,C₁-C₆-haloalkyl, C₂-C₆-alkenyl, C₂-C₆-haloalkenyl, C₂-C₆-alkynyl,C₃-C₆-haloalkynyl, C₃-C₆-cycloalkyl, C₃-C₆-cycloalkenyl,C₃-C₆-halocycloalkyl, C₃-C₆-cycloalkyl-C₁-C₆-alkyl,C₁-C₆-alkoxy-C₁-C₆-alkyl, C₃-C₆-cycloalkyl-C₁-C₆-alkoxy-C₁-C₆-alkyl,phenyl, phenyl-C₁-C₆-alkyl, heteroaryl, heteroaryl-C₁-C₆-alkyl,heterocyclyl, heterocyclyl-C₁-C₆-alkyl, phenyl-O—C₁-C₆-alkyl,heteroaryl-O—C₁-C₆-alkyl, heterocyclyl-O—C₁-C₆-alkyl,phenyl-N(R²³)—C₁-C₆-alkyl, heteroaryl-N(R²³)—C₁-C₆-alkyl,heterocyclyl-N(R²³)—C₁-C₆-alkyl, phenyl-S(O)_(n)—C₁-C₆-alkyl,heteroaryl-S(O)_(n)—C₁-C₆-alkyl, heterocyclyl-S(O)_(n)—C₁-C₆-alkyl,where the 15 aforementioned radicals are substituted by s residuesselected from the group consisting of nitro, halogen, cyano, rhodano,C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₃-C₆-cycloalkyl, C(O)OR²³, C(O)N(R²³)₂,OR²³, N(R²³)₂, S(O)_(n)R²⁴, S(O)₂OR²³, S(O)₂N(R²³)₂ andR²³O—C₁-C₆-alkyl, and where heterocyclyl bears 0, 1 or 2 oxo groups; R²⁶is C₁-C₆-alkyl or C₁-C₄-alkoxy-C₁-C₄-alkyl; R²⁷ is selected from thegroup consisting of hydrogen, cyano and C₁-C₄-haloalkylcarbonyl; R²⁸,R²⁹ independently of each other are C₁-C₆-alkyl, or R²⁸, R²⁹ togetherwith the sulfur atom, to which they are bound may form a 5- or6-membered saturated ring, which may carry as a ring member 1 oxygenatom; k is 0, 1 or 2; n is 0, 1 or 2; s is 0, 1, 2 or 3; t is 0 or 1.33. The compound of claim 32, an N-oxide or an agriculturally suitablesalt thereof, wherein B is N.
 34. The compound of claim 32, an N-oxideor an agriculturally suitable salt thereof, wherein B is CH.
 35. Thecompound of claim 32, an N-oxide or an agriculturally suitable saltthereof, wherein R¹ is selected from the group consisting of cyano,halogen, nitro, C₁-C₆-alkyl, C₃-C₆-cycloalkyl, C₂-C₆-alkenyl,C₂-C₆-alkynyl, C₁-C₆-haloalkyl, C₁-C₆-alkoxy, C₁-C₄-alkoxy-C₁-C₄-alkyl,C₁-C₄-haloalkoxy-C₁-C₄-alkyl, C₁-C₄-alkoxy-C₁-C₄-alkoxy-Z¹,C₁-C₄-alkylthio-C₁-C₄-alkyl, C₁-C₄-alkylthio-C₁-C₄-alkylthio-Z¹,C₂-C₆-alkenyloxy, C₂-C₆-alkynyloxy, C₁-C₆-haloalkoxy,C₁-C₄-haloalkoxy-C₁-C₄-alkoxy and R^(1b)—S(O)_(k), wherein Z¹ is asdefined in claim 33, wherein k is 0, 1 or 2 and wherein R^(1b) isselected from the group consisting of C₁-C₄-alkyl and C₁-C₄-haloalkyl.36. The compound of claim 32, an N-oxide or an agriculturally suitablesalt thereof, wherein R¹ is selected from the group consisting ofhalogen, CN, nitro, C₁-C₄-alkyl, C₃-C₆-cycloalkyl, C₁-C₄-haloalkyl,C₁-C₄-alkoxy-C₁-C₄-alkyl, C₁-C₄-haloalkoxy-C₁-C₄-alkyl,C₁-C₄-alkoxy-C₁-C₄-alkoxy-C₁-C₄-alkyl, C₁-C₄-alkylthio-C₁-C₄-alkyl,C₁-C₄-alkylthio-C₁-C₄-alkylthio-C₁-C₄-alkyl, C₁-C₄-alkoxy,C₁-C₄-haloalkoxy, C₃-C₄-alkenyloxy, C₃-C₄-alkynyloxy,C₁-C₄-alkoxy-C₁-C₄-alkoxy, C₁-C₄-haloalkoxy-C₁-C₄-alkoxy,C₁-C₄-alkyl-S(O)_(k) and C₁-C₄-haloalkyl-S(O)_(k), wherein k is 0 or 2.37. The compound of claim 32, an N-oxide or an agriculturally suitablesalt thereof, wherein R¹ is selected from the group consisting ofhalogen, nitro, C₁-C₄-alkyl, C₃-C₆-cycloalkyl, C₁-C₄-haloalkyl,C₁-C₄-alkoxy-C₁-C₄-alkyl, C₁-C₄-alkoxy-C₁-C₄-alkoxy-C₁-C₄-alkyl,C₁-C₄-alkoxy, C₁-C₄-haloalkoxy, C₁-C₄-alkylthio, C₁-C₄-haloalkylthio andC₁-C₄-alkylsulfonyl.
 38. The compound of claim 32, an N-oxide or anagriculturally suitable salt thereof, wherein X is N.
 39. The compoundof claim 32, an N-oxide or an agriculturally suitable salt thereof,wherein X is CR² and R² is not hydrogen.
 40. The compound of claim 32,an N-oxide or an agriculturally suitable salt thereof, wherein X is CR²and R² is hydrogen.
 41. The compound of claim 32, an N-oxide or anagriculturally suitable salt thereof, wherein R² is 5- or 6-memberedheterocyclyl, wherein heterocyclyl is a saturated, partially unsaturatedor aromatic heterocyclic radical, which contains as a ring member 1heteroatom selected from the group consisting of O, N and S and 0, 1, 2or 3 further nitrogen atoms, wherein heterocyclyl is unsubstituted orcarries 1, 2 or 3 radicals R²¹ which are identical or different.
 42. Thecompound of claim 32, an N-oxide or an agriculturally suitable saltthereof, wherein R² is 5- or 6-membered heterocyclyl selected from thegroup consisting of isoxazolinyl, 1,2-dihydrotetrazolonyl,1,4-dihydrotetrazolonyl, tetrahydrofuryl, dioxolanyl, piperidinyl,morpholinyl, piperazinyl, isoxazolyl, pyrazolyl, thiazolyl, oxazolyl,furyl, pyridinyl, pyrimidinyl and pyrazinyl, wherein heterocyclyl isunsubstituted or carries 1, 2 or 3 radicals R²¹ which are identical ordifferent and selected from the group consisting of C₁-C₄-alkyl,C₁-C₄-haloalkyl, C₁-C₄-alkoxy, C₁-C₄-alkoxy-C₁-C₄-alkyl andC₁-C₄-alkylthio-C₁-C₄-alkyl.
 43. The compound of claim 32, an N-oxide oran agriculturally suitable salt thereof, wherein R² is selected from thegroup consisting of hydrogen, halogen, C₁-C₆-alkyl,C₃-C₆-cycloalkyl-C₁-C₄-alkoxy, C₁-C₄-alkoxy-C₁-C₄-alkyl,C₁-C₄-haloalkoxy-C₁-C₄-alkyl, C₂-C₆-alkenyl, C₂-C₆-alkynyl,C₁-C₄-alkoxy, C₁-C₄-haloalkoxy, C₃-C₆-alkenyloxy, C₃-C₆-alkynyloxy,C₃-C₆-haloalkenyloxy, C₃-C₆-haloalkynyloxy, C₁-C₄-alkoxy-C₁-C₄-alkoxy,C₁-C₄-alkoxycarbonyl, C₁-C₄-alkyl-S(O)_(k) and C₁-C₄-haloalkyl-S(O)_(k),wherein k is 0, 1 or 2, N(C₁-C₄-alkyl)SO₂(C₁-C₄-alkyl), isoxazolyl andisoxazolinyl, wherein the last two mentioned radicals may beunsubstituted or carry 1 or 2 radicals selected from the groupconsisting of halogen and C₁-C₄-alkyl.
 44. The compound of claim 32, anN-oxide or an agriculturally suitable salt thereof, wherein R² is

wherein R²⁶ is selected from the group consisting of methyl, ethyl andmethoxyethyl, R²⁷ is selected from the group consisting of hydrogen,cyano and trifluoroacetyl, t is 0 or 1; or

wherein R²⁸ is ethyl and R²⁹ is ethyl, or R²⁸ and R²⁹ together are—(CH₂)₅— or —(CH₂)₂—O—(CH₂)₂—.
 45. The compound of claim 32, an N-oxideor an agriculturally suitable salt thereof, wherein R³ is selected fromthe group consisting of hydrogen, halogen, cyano, nitro, C₁-C₄-alkyl,C₁-C₄-haloalkyl, C₁-C₄-alkoxy, C₁-C₄-haloalkoxy, C₂-C₄-alkenyl,C₂-C₄-alkynyl, C₃-C₄-alkenyloxy, C₃-C₄-alkynyloxy or R^(2b)—S(O)_(k),where k is 0, 1 or 2 and wherein R^(2b) is selected from the groupconsisting of C₁-C₄-alkyl and C₁-C₄-haloalkyl.
 46. The compound of claim32, an N-oxide or an agriculturally suitable salt thereof, wherein R³ isselected from the group consisting of hydrogen, halogen, cyano, nitro,C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy, C₁-C₄-haloalkoxy,C₁-C₄-alkylthio, C₁-C₄-haloalkylthio, C₁-C₄-alkyl-S(O)₂ andC₁-C₄-haloalkyl-S(O)₂.
 47. The compound of claim 32, an N-oxide or anagriculturally suitable salt thereof, wherein R⁴ is selected from thegroup consisting of hydrogen, CHF₂, CF₃, CN, NO₂, CH₃ and halogen. 48.The compound of claim 32, an N-oxide or an agriculturally suitable saltthereof, wherein R⁵ is selected from the group consisting of CHF₂, CF₃and halogen.
 49. The compound of claim 32, an N-oxide or anagriculturally suitable salt thereof, wherein R⁶ is selected from thegroup consisting of cyano, C₁-C₆-alkyl, C₁-C₆-cyano-alkyl, C₁-C₆-alkoxy,C₂-C₆-alkenyl, C₂-C₆-haloalkenyl, C₂-C₆-alkynyl, C₂-C₆-haloalkynyl,C₁-C₄-alkoxy-C₁-C₄-alkyl, C₁-C₄-haloalkoxy-C₁-C₄-alkyl,R^(b)R^(b)N—S(O)_(n)—Z, R^(b)O—S(O)_(n)—Z, R^(b)—S(O)_(n)—Z,R^(d)—C(═O)O—C₁-C₃-alkyl, C(═O)O(═O)O—C₁-C₃-alkyl,R^(d)O—C(═O)—C₁-C₃-alkyl, R^(e)R^(f)N—C(═O)—C₁-C₃-alkyl, phenyl-Z andwherein phenyl is unsubstituted or substituted by 1, 2, 3 or 4 groupsR′, which are identical or different.
 50. The compound of claim 32, anN-oxide or an agriculturally suitable salt thereof, wherein R⁶ isselected from the group consisting of C₁-C₆-alkyl, C₂-C₆-alkenyl,C₂-C₆-alkynyl, C₁-C₄-alkoxy-C₁-C₄-alkyl, R^(d)O—C(═O)—C₁-C₃-alkyl,phenyl-Z and wherein phenyl is unsubstituted or substituted by 1, 2, 3or 4 groups R′, which are identical or different.
 51. The compound ofclaim 23, an N-oxide or an agriculturally suitable salt thereof, whereinR⁷ is selected from the group consisting of C₁-C₄-alkyl,C₃-C₇-cycloalkyl, C₁-C₄-haloalkyl, C₂-C₆-alkenyl, C₂-C₆-alkynyl, andC₁-C₄-alkoxy-C₁-C₄-alkyl.
 52. The compound of claim 32, an N-oxide or anagriculturally suitable salt thereof, wherein R¹ is selected from thegroup consisting of halogen, nitro, C₁-C₄-alkyl, C₃-C₆-cycloalkyl,C₁-C₄-haloalkyl, C₁-C₄-alkoxy-C₁-C₄-alkyl,C₁-C₄-alkoxy-C₁-C₄-alkoxy-C₁-C₄-alkyl, C₁-C₄-alkoxy, C₁-C₄-haloalkoxy,C₁-C₄-alkylthio, C₁-C₄-haloalkylthio and C₁-C₄-alkylsulfonyl; and R³ isselected from the group consisting of hydrogen, halogen, cyano, nitro,C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy, C₁-C₄-haloalkoxy,C₁-C₄-alkylthio, C₁-C₄-haloalkylthio and C₁-C₄-alkylsulfonyl.
 53. Thecompound of claim 32, an N-oxide or an agriculturally suitable saltthereof, wherein X is CR² and the variables R¹, R², R³, R⁴, R⁵, R⁶ andR⁷ have the following meanings: R¹ is selected from the group consistingof halogen, nitro, cyclopropyl, C₁-C₄-alkyl, C₁-C₄-haloalkyl,C₁-C₄-alkoxy-C₁-C₄-alkyl, C₁-C₄-alkoxy-C₁-C₄-alkoxy-C₁-C₄-alkyl andC₁-C₄-alkyl-S(O)₂; R² is selected from the group consisting of hydrogen,halogen, C₁-C₄-alkyl, C₁-C₄-alkoxy, C₁-C₄-haloalkoxy,C₃-C₆-cycloalkyl-C₁-C₂-alkoxy, C₁-C₂-alkoxy-C₁-C₂-alkyl,C₁-C₂-haloalkoxy-C₁-C₂-alkyl, C₁-C₂-alkoxy-C₁-C₂-alkoxy,C₁-C₄-alkyl-S(O)_(k), where k is 0, 1 or 2,N(C₁-C₄-alkyl)SO₂(C₁-C₄-alkyl), isoxazolyl and isoxazolinyl, where thelast two mentioned radicals may be unsubstituted or carry 1 or 2radicals selected from halogen and C₁-C₄-alkyl; R³ is selected from thegroup consisting of hydrogen, halogen, cyano, nitro, C₁-C₄-alkyl,C₁-C₄-haloalkyl and C₁-C₄-alkyl-S(O)₂; R⁴ is selected from the groupconsisting of hydrogen, cyano, methyl and halogen; R⁵ is selected fromthe group consisting of halogen, CHF₂ and CF₃; R⁶ is selected from thegroup consisting of C₁-C₄-alkyl, C₁-C₂-alkoxy-C₁-C₂-alkyl,C₂-C₄-alkenyl, C₂-C₄-alkynyl, C₁-C₄-alkoxycarbonyl-C₁-C₄-alkyl andphenyl-C₁-C₂-alkyl; R⁷ is selected from the group consisting ofC₁-C₄-alkyl and C₁-C₂-alkoxy-C₁-C₂-alkyl.
 54. The compound of claim 32,an N-oxide or an agriculturally suitable salt thereof, wherein X is CR²and the variables R¹, R², R³, R⁴, R⁵, R⁶ and R⁷ have the followingmeanings: R¹ is selected from the group consisting of chlorine, nitro,methyl, cyclopropyl, trifluoromethyl, methoxymethyl, CH₂OCH₂CH₂OCH₃ andmethylsulfonyl; R² is selected from the group consisting of hydrogen,chlorine, fluorine, methyl, methoxy, ethoxy, OCH₂(cyclo-C₃H₅), OCHF₂,OCH₂CF₃, OCH₂CH₂OCH₃, methoxymethyl, CH₂OCH₂CF₃, methylsulfonyl,ethylsulfonyl, methylsulfinyl, ethylsulfinyl, methylsulfanyl,ethylsulfanyl, NCH₃SO₂CH₃, 3-isoxazolinyl, 5-methyl-3-isoxazolinyl,5-isoxazolinyl, 3-methyl-5-isoxazolinyl, 3-isoxazolyl,5-methyl-3-isoxazolyl, 5-isoxazolyl and 3-methyl-5-isoxazolyl; R³ isselected from the group consisting of hydrogen, fluorine, chlorine,bromine, cyano, nitro, methyl, trifluoromethyl and methylsulfonyl; R⁴ isselected from the group consisting of hydrogen, cyano, methyl, chlorineand fluorine; R⁵ is selected from the group consisting of chlorine andfluorine; R⁶ is selected from the group consisting of methyl, ethyl,methoxymethyl, ethoxymethyl, prop-2-enyl, prop-2-ynyl,methoxycarbonylmethyl and benzyl; R⁷ is selected from the groupconsisting of methyl, ethyl, propyl, methoxymethyl, methoxyethyl andethoxymethyl.
 55. The compound of claim 21, an N-oxide or anagriculturally suitable salt thereof, wherein X is N and the variablesR¹, R³, R⁴, R⁵, R⁶ and R⁷ have the following meanings: R¹ is selectedfrom the group consisting of halogen, nitro, cyclopropyl, C₁-C₄-alkyl,C₁-C₄-haloalkyl, C₁-C₄-alkoxy-C₁-C₄-alkyl,C₁-C₄-alkoxy-C₁-C₄-alkoxy-C₁-C₄-alkyl and C₁-C₄-alkyl-S(O)₂; R³ isselected from the group consisting of hydrogen, halogen, cyano, nitro,C₁-C₄-alkyl, C₁-C₄-haloalkyl and C₁-C₄-alkyl-S(O)₂; R⁴ is selected fromthe group consisting of hydrogen, cyano, methyl and halogen; R⁵ isselected from the group consisting of halogen, CHF₂ and CF₃; R⁶ isselected from the group consisting of C₁-C₄-alkyl,C₁-C₂-alkoxy-C₁-C₂-alkyl, C₂-C₄-alkenyl, C₂-C₄-alkynyl,C₁-C₄-alkoxycarbonyl-C₁-C₄-alkyl and phenyl-C₁-C₂-alkyl; R⁷ is selectedfrom the group consisting of C₁-C₄-alkyl and C₁-C₂-alkoxy-C₁-C₂-alkyl.56. The compound of claim 32, an N-oxide or an agriculturally suitablesalt thereof, wherein X is N and the variables R¹, R³, R⁴, R⁵, R⁶ and R⁷have the following meanings: R¹ is selected from the group consisting ofchlorine, nitro, methyl, cyclopropyl, trifluoromethyl, methoxymethyl,CH₂OCH₂CH₂OCH₃ and methylsulfonyl; R³ is selected from the groupconsisting of hydrogen, fluorine, chlorine, bromine, cyano, nitro,methyl, trifluoromethyl and methylsulfonyl; R⁴ is selected from thegroup consisting of hydrogen, cyano, methyl, chlorine and fluorine; R⁵is selected from the group consisting of chlorine and fluorine; R⁶ isselected from the group consisting of methyl, ethyl, methoxymethyl,ethoxymethyl, prop-2-enyl, prop-2-ynyl, methoxycarbonylmethyl andbenzyl; R⁷ is selected from the group consisting of methyl, ethyl,propyl, methoxymethyl, methoxyethyl and ethoxymethyl.
 57. The compoundof claim 32, an N-oxide or an agriculturally suitable salt thereof,wherein X is CR² and the variables R¹, R², R³, R⁴, R⁵, R⁶ and R⁷ havethe following meanings: R¹ is selected from the group consisting ofchlorine, nitro, methyl, cyclopropyl, trifluoromethyl, methoxymethyl,CH₂OCH₂CH₂OCH₃ and methylsulfonyl; R² is selected from the groupconsisting of hydrogen, chlorine, fluorine, methyl, CH₂OCH₂CF₃,methylsulfonyl, ethylsulfonyl, methylsulfanyl, ethylsulfanyl,3-isoxazolinyl, 5-methyl-3-isoxazolinyl, 5-isoxazolinyl,3-methyl-5-isoxazolinyl, 3-isoxazolyl, 5-methyl-3-isoxazolyl,5-isoxazolyl and 3-methyl-5-isoxazolyl; R³ is selected from the groupconsisting of hydrogen, fluorine, chlorine, cyano, nitro, methyl,trifluoromethyl and methylsulfonyl; R⁴ is selected from the groupconsisting of hydrogen, cyano, methyl, chlorine and fluorine; R⁵ isselected from the group consisting of chlorine and fluorine; R⁶ isselected from the group consisting of methyl, ethyl, methoxymethyl,ethoxymethyl, prop-2-ynyl and methoxycarbonylmethyl; R⁷ is selected fromthe group consisting of methyl, ethyl and methoxyethyl.
 58. The compoundof claim 32, an N-oxide or an agriculturally suitable salt thereof,wherein X is CR² and the variable R³ is not hydrogen.
 59. The compoundof claim 32, an N-oxide or an agriculturally suitable salt thereof,wherein X is CR² and the variables R² and R³ are not hydrogen.
 60. Acomposition comprising at least one compound of claim 32, an N-oxide oran agriculturally suitable salt thereof, and at least one auxiliary,which is customary for formulating crop protection compounds.
 61. Amethod for controlling unwanted vegetation, comprising allowing aherbicidally effective amount of at least one compound of claim 32, anN-oxide or an agriculturally suitable salt thereof, to act on plants,their seed, their habitat, or on a combination of two or all thereof.62. A method for controlling unwanted vegetation, comprising allowing aherbicidally effective amount the composition of claim 60 to act onplants, their seed, their habitat, or on a combination of two or allthereof.